Setubal Clinical Medical Research Job Listings

Data & AI Platform/Solution Architect Master

Noesis is seeking professionals with the following profile: **Responsibilities**: * Model business requirements — data dimension — into normalized, denormalized, star-schema, or other data models aligned with objectives; * Model business requirements into non-tabular data models: columnar, graph, geospatial, time-series, document; * Model business requirements including data streams and integrations (schema API, CRUD API); * Design data models and data architecture to meet qualitative requirements: cost, write performance, indexed GET queries, scans, feature retrieval (advanced analytical queries), usage elasticity (scale up, scale-out, pause); * Design and implement reference data architectures according to data governance strategy requirements; * Design and implement blueprints for the organizational data framework — defining how data is acquired, stored, consumed, integrated, and managed to enrich the company’s Data Lakes, MDUs, and Data Marts; * Define indicators related to DataOps absorbability, organized across three dimensions: * 1) Operational health of data pipelines (duration, latency, retries, time between successive executions); * 2) Dataset-level health (availability, freshness, volume, schema changes); * 3) Data-level health (profiling within “expectation envelope”, outlier and anomaly detection, data drift, and business rule enforcement); * Ensure technical capabilities (e.g., scalability, security, performance, data recovery, reliability, etc.); * Apply best practices in data governance and data security: data catalog, data lineage, data quality, master data management, metadata management, data standards; * Prepare business process reports; * Perform corrections and enhancements to the Celonis platform; * Conduct technical analyses of functionalities for inclusion of new processes in Celonis. **Requirements**: * Bachelor’s degree in Software Engineering, Computer Engineering, or equivalent; * Over 5 years of experience as a Data & AI Platform / Solution Architect Specialist; * Up-to-date knowledge of databases and analytical technologies, including data lake / lakehouse architectures and NoSQL storage; * Experience with Cloud Platforms (one or more: AWS, Google Cloud, Azure); * Knowledge of data governance and data security practices; * Knowledge of Machine Learning, algorithms, and statistical models (e.g., classification, time-series analysis, regression, …); * Experience in metadata management, data catalogs, data standards, and best practices in master data management; * Experience with Big Data databases (one or more: BigQuery, Azure Synapse, AWS RedShift, Cassandra, Couchbase, HDFS); * CELONIS certification; * Proven experience implementing Celonis technology; * Knowledge of the Energy & Utilities market and GDPR; * Ability to work collaboratively in global teams; * Critical analytical skills and problem-solving focus; * Familiarity with Agile methodology, JIRA, and Confluence (valued); * Language proficiency (written and spoken): English (mandatory), Portuguese (preferred), Spanish (preferred). If you meet these criteria and wish to join an innovative organization that continuously invests in developing its talent, submit your application here > Data & AI Platform/Solution Architect Master **Join us. Let’s innovate together!** All our recruitment and selection processes are based on equal opportunity principles, valuing each individual’s competence and potential, and ensuring no candidate is discriminated against on grounds of gender, ethnicity, sexual orientation, age, religion, or physical condition. * This announcement complies with Law No. 4/2019, dated January 10 The original job posting can be found at: https://www.itjobs.pt/oferta/507937/data-ai-platform-solution-architect-master

PV49+C7 Lisbon, Portugal

Negotiable Salary

Indeed

Area Coordinator

#### **Your day\-to\-day** * I participate in setting short\- to medium\-term objectives and strategy for the Area; * I proactively analyze and monitor the Area's results, tracking and reviewing the Profit and Loss statement, identifying improvement opportunities, analyzing variances, and driving appropriate action plans to minimize losses. * I continuously monitor business development, analyzing data and key indicators to proactively take necessary actions and initiatives to achieve tactical and operational goals; * I understand market potential and consumer behavior in my region, identify customer needs, and implement action plans accordingly; * I ensure effective product offering management and coordinate efficient collection rollouts, guaranteeing time to market; * I work closely with the space and stock team, proactively identifying section purchasing needs and contributing to product availability on shelves; * I participate in recruiting my team, support them in their daily activities, and contribute to developing their skills. #### **What we are looking for** * Secondary education (12th grade or equivalent); * Experience in Sales Team Management (preferably in Retail); * Proactivity and sense of responsibility; * Initiative and entrepreneurial mindset; * Ability to work autonomously and make decisions; * Strong interpersonal and teamwork skills; * Good communication, negotiation, and influencing abilities; * Knowledge of English. **What we offer** * Integration into a multinational company with competitive salary and variable compensation tailored to your experience and qualifications; * Benefits and partnerships with over 200 brands; * Initial training for onboarding into the company and role; * Well\-being policies, including up to 30 days of annual leave; * Employee referral program with incentives for each recommended candidate hired; * Flexible working policy; * Meal benefits, including provision of soup, fresh fruit, bread, butter, cereals, milk, and yogurts; * 10% discount at Leroy Merlin stores; * Health and life insurance; * 1 corporate volunteering day. #### **About us** Leroy Merlin is a leading company in DIY, construction, decoration, and gardening, with a strong presence in Portugal. Committed to innovation, sustainability, and customer experience, we offer a dynamic and collaborative work environment where we value diversity, creativity, and proactivity. We place people at the heart of every decision and embrace a Human First culture, where every employee is a leader with the opportunity to grow.

G3CF+2C Setúbal, Portugal

Negotiable Salary

Experienced Clinical Research Associate - based in Portugal64628147407490122

Indeed

Experienced Clinical Research Associate - based in Portugal

**Senior Clinical Research Associate** **Your responsibilities will include:** * Performing site selection, initiation, monitoring and close\-out visits * Supporting the development of a subject recruitment plan * Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines * Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions * Collaborating with experts at study sites and with client representatives **Qualifications:** * University degree in scientific discipline or health care * Requires at least 3 year of on\-site monitoring experience. * Very good computer skills including MS Office * Excellent command of Portuguese and English language. * Organizational, time management and problem\-solving skills * Ability to establish and maintain effective working relationships with coworkers, managers, and clients * Flexibility to travel * Driver’s license class B **What you can expect:** * Resources that promote your career growth * Leaders that support flexible work schedules * Programs to help you build your therapeutic knowledge * Excellent working environment in a stabile, international, reputable company * Company car, mobile phone and attractive benefits package IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi\-talented collaboration harnesses innovation to deliver superior outcomes.

R. António Sérgio 5, 2780-199 Oeiras, Portugal

Negotiable Salary

Indeed

Full-Stack Developer

AQUASIS develops innovative applications and technological solutions for engineering problem analysis, planning, and support of management, operation, and maintenance of systems related to the Urban Water Cycle. We connect business process knowledge, cutting-edge technologies, and passion for innovation. If you share a passion for innovation and wish to turn your career goals in the IT field into reality, AQUASIS has an opportunity for you! We are seeking to strengthen our team with a Full-Stack Developer position. **What we are looking for?** * Academic background: Bachelor’s degree in Computer Engineering or equivalent; * Development experience with the following technologies: JavaScript, React.js, TypeScript, REST APIs, GitHub, HTML5, CSS 3.0, ASP.NET (C#), Entity Framework, .NET Core; * Knowledge of SQL databases: Oracle, SQL Server, or PostgreSQL; * Proficiency in spoken and written English; * Minimum of 3 years’ professional experience in development projects in Portugal; **What we offer?** * Integration into a solid and dynamic team; * Opportunity to participate in international projects; * Involvement in exciting and motivating projects with leading clients; * Hybrid work regime; * Competitive salary package aligned with profile and experience; * Health insurance; * Workplace location: Oeiras. Send your CV to \ and join the AQUASIS team! The original job posting can be found at: https://www.itjobs.pt/oferta/507687/fullstack\-developer

PV49+C7 Lisbon, Portugal

Negotiable Salary

Senior Statistical Analyst64538792158979124

Indeed

Senior Statistical Analyst

JR136668 Senior Statistical Analyst ICON plc is a world\-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Senior Statistical Analyst to join our diverse and dynamic team. As a Senior Statistical Analyst at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What you will be doing* Collaborating with cross\-functional teams to design statistical methodologies and analysis plans for clinical trials. * Conducting statistical analyses and interpreting results to support decision\-making and regulatory submissions. * Developing and validating statistical models to analyze clinical trial data and evaluate treatment outcomes. * Providing statistical expertise and guidance to support study design, protocol development, and data interpretation. * Contributing to the development of statistical analysis protocols and programming specifications. Your profile* Master's or Ph.D. degree in Statistics, Biostatistics, or related field. * Minimum of 5 years of experience in statistical analysis within the pharmaceutical, biotechnology, or CRO industry. * Proficiency in statistical software such as SAS, R, or Python. * Strong understanding of clinical trial design, statistical methodologies, and regulatory requirements. * Excellent analytical, problem\-solving, and communication skills. \#LI\-SA1 What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well\-being and work life balance opportunities for you and your family. Our benefits examples include:* Various annual leave entitlements * A range of health insurance offerings to suit you and your family’s needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, TELUS Health, offering 24\-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well\-being. * Life assurance * Flexible country\-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion \& belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

PV49+C7 Lisbon, Portugal

Negotiable Salary

Indeed

Data Engineer

**We want to do different with the essential’s things.** We are committed to a sustainable corporatism strategy. We believe that success is based on building a team focused on collective well\-being, personal and professional development, and based on a work philosophy that enhances the healthy management of our lives. Work\-life balance, beginner’s mind and community involvement are our identity, our foundations, and our culture. ***What you need to join us:*** * Bachelor’s degree in information systems, Computer Science, Engineering, or other related. * 2\+ years of professional consulting experience in technology consulting or similar roles. * Good understanding of ETL, ELT, data ingestion/cleansing and engineering skills * Azure Databricks, PySpark, SQL and/or Python. * Data Ingestion and Storage. Preferably in Azure Data Factory, Azure Data Lake. * Experience with DevOps, CI/CD, Agile and/or Scrum methods of delivery * MS Certifications: Azure Data Engineer Associate, Azure Fundamentals * Experience in Cosmos DB, Synapse, APIs, Azure ML. * Excellent English communication skills (written \& spoken) ***What do we have to offer you:*** * **Personalized Talent Management**. We value and privilege a close and regular follow\-up; we are a team from day one. * **Broad and flexible benefits package.** Health insurance, life and personal accident insurance, discounts and benefits, telecommunications plan and much more. * **We invest in training and in your career**. Certified training, online training platforms, Pearson VUE exam center... We bet on you! * **Sustainability and community involvement.** We want to give meaning to our work and invest in an inclusive consulting project. For that, we need your help. ***team.it, back to basics!*** Will you join us? *At Team IT we defend equality and value diversity.* *We create a safe, diverse environment where opportunities are equal for everyone!* *We do not discriminate based on age, ethnicity, sexual orientation, gender, disability, or any factor other than merit.* *All applications with skills for the position are welcome!* Apply here Poderá encontrar o anúncio original publicado em: https://www.itjobs.pt/oferta/507231/data\-engineer

PV49+C7 Lisbon, Portugal

Negotiable Salary

Indeed

Nursing

**Offer Code:**OE202511/0323 **Type of Offer:**Public Competition Procedure for Establishing a Recruitment Reserve Pool **Status:**Active **Organizational Level:**Ministry of Health **Organization/Service:**Unidade Local de Saúde de Loures\-Odivelas, E.P.E. **Employment Type:**Indefinite-term employment contract/Open-ended employment contract **Regime:**Special Careers **Career:**Nursing **Category:**Nurse **Level of Complexity:**0 **Remuneration:**1\.547,83€ **Monthly Supplement:**0.00 EUR **Job Position Description:**PUBLIC COMPETITION PROCEDURE FOR ESTABLISHING A RECRUITMENT RESERVE POOL FOR NURSES **Work Location** **Address** **Locality** **Postal Code** **District** **Municipality** Unidade Local de Saúde de Loures\-Odivelas, E.P.E. Avenida Carlos Teixeira, n.º 3 Loures 2674514 LOURES Lisboa Loures **Quota for Disabled Candidates:**0

PV49+C7 Lisbon, Portugal

€ 1,547/month

Performance Marketing Specialist64411371737858127

Indeed

Performance Marketing Specialist

**ComparaJá: Accelerate Your Career. Accelerate Our Results!** ComparaJá is the largest digital financial services platform in Portugal, and we are changing the way families make decisions. To continue growing, we need a **Performance Marketing Specialist** who will be the **Owner** of our *lead* acquisition in the **Energy** and **Telecom** verticals. If your focus is **profitability** and your language is **Excel**, we want to talk to you! **Responsibilities:** You will be primarily responsible for ensuring that our digital campaigns generate not only volume but do so with the right profitability. Additionally, your focus will include: * **Strategy \& Execution:** Plan, execute, and optimize all campaigns across Performance Marketing channels (Google Ads, Meta Ads, and others). * **Data Analysis:** Dive deep into data to identify *bottlenecks*, solve performance issues, and uncover new opportunities for growth and efficiency; **Identifying new channels: Explore new business growth opportunities, becoming the internal expert on these channels;** * **Results:** Ensure achievement of the defined **Lead Target** for the Energy and Telecommunications verticals. **Requirements:** * **Analytical with a touch of creativity:** Proven ability to extract meaningful *insights* from large volumes of data, as well as understanding which creatives work and ensuring produced creatives align with best practices. **Being an analytical person is essential.** * **Excel proficiency:** Excel is your daily working tool. * **Technical Experience:** Solid knowledge and hands-on experience with **Google Ads** and **Meta Ads**. * **Bonus:** Knowledge of **TikTok Ads** or other emerging *performance* channels. * **Problem Solving:** Strong ability to quickly identify campaign issues and propose concrete, data-driven solutions. **Why ComparaJá?** * **Real Impact:** You’ll work in essential sectors (Energy and Telecommunications), helping thousands of people make better financial decisions. * **FinTech Culture:** A dynamic work environment focused on technology, methodology, and continuous improvement. * **Development:** Continuous learning alongside a team of Marketing and Finance experts. **Want to be the*** ***Driver*** **of performance in our project? Apply now!** Type of offer: Full-time Benefits: * Meal voucher/Meal card * Health insurance

PV49+C7 Lisbon, Portugal

Negotiable Salary

Indeed

Clinical Trial Manager

Local Trial Manager ICON plc is a world\-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for overseeing the planning, execution, and successful completion of clinical trials, ensuring adherence to timelines, budgets, and regulatory guidelines. As a leader in our research department, you will collaborate with cross\-functional teams, manage site relationships, and provide strategic guidance to drive the successful delivery of clinical trial outcomes. What you will be doing* Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards. * Collaborate with cross\-functional teams to establish and implement clinical trial protocols and procedures. * Build and manage strong relationships with trial investigators and stakeholders. * Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines. * Problem\-solve and make critical decisions regarding trial design, vendor selection, and risk management. Your Profile* University degree in medicine, science, or equivalent combination of education \& experience * Demonstrated ability to drive the clinical deliverables of a study * Subject matter expertise in the designated therapeutic area * Prior monitoring experience is preferred * Ability to travel up to 20% What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well\-being and work life balance opportunities for you and your family. Our benefits examples include:* Various annual leave entitlements * A range of health insurance offerings to suit you and your family’s needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, TELUS Health, offering 24\-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well\-being. * Life assurance * Flexible country\-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion \& belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

PV49+C7 Lisbon, Portugal

Negotiable Salary

Manager, Site Contracts ** open to several EMEA countries **64373352706689129

Indeed

Manager, Site Contracts ** open to several EMEA countries **

**Description** Manager, Site Contracts \*\* open to several EMEA countries \*\* Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** **JOB SUMMARY** Assists senior management in managing work and teams within a specific or broad area of site start\-up, such as site activation, regulatory/ethics submissions, site contracts, and/or life cycle maintenance activities. Ensures fulfillment of customer requirements and compliance with related regulations. Analyzes processes to increase efficiency. Performs operational level planning, including efficient allocation of resources within the department. Participates in business development presentations as a subject matter expert in Site Start\-Up \& Regulatory functions within the Company. **JOB RESPONSIBILITIES** * Conducts people management activities including interviewing and selection, terminations, professional development, performance appraisals, job description preparation, and employee counseling. * Provides guidance on administrative policies and procedures, technical problems, priorities, and methods. * Acts as liaison and facilitator between customer leaders and senior management for related tasks and/or issues. Plans and negotiates resources with line management of functional areas. * Supports management with site start\-up or maintenance and financial management tasks of projects, as well as strategy development for process improvement. Facilitates and supports project reviews with Clinical Operations staff, focusing on budget, schedule, and risk analysis. * Supports management in reviewing, approving, and presenting prepared information at project or departmental review meetings. Develops and implements training programs for appropriate departmental teams. * Interacts with the executive management and Legal Department and assists with the accurate creation and implementation of site contracts, site start\-up, maintenance and regulatory management workflows. Identifies and reports on areas of process and risk. * Implements customer\-required and/or enterprise\-wide project management systems and tools. Participates in the development, implementation, and maintenance of enterprise project management systems, acting as a systems manager; may supervise a systems administrator. * Develops requirements for modifications to existing systems and reports based on input from functional teams. Provides input and requirements for long\-range IT plans. Implements Company and customer\-required project management systems and processes. * Leads teams of subject matter experts in the development and review of Standard Operating Procedures (SOPs) and Work Instructions (WI) to support new or existing processes. Develops and implements strategies and tools for tracking contract management team metrics/cycle times. Oversees all quality control efforts of individual departmental teams. * Represents the Company at professional meetings or seminars. * Establishes and maintains training materials for assigned area. **QUALIFICATION \& REQUIREMENTS** * Bachelor’s Degree. * Experience in a clinical research organization and related contract management or site start\-up experience. * Background in development/management of information systems and process engineering preferred. * Thorough knowledge of applicable regulations, drug development, and clinical project management procedures. * Strong presentation, documentation, and interpersonal skills. * Proficient in MS Office (Word, Excel, and PowerPoint), MS Project, email, and Internet. * Ability to handle multiple tasks to meet deadlines, delivering high quality work in a dynamic environment. * Demonstrate line management abilities. * Strong leadership skills; ability to teach/mentor team members. * Ability to coach employees to reach performance objectives. * Ability to recognize and take appropriate action when employee performance is not acceptable. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Av. João Crisóstomo 57, 1050-126 Lisboa, Portugal

Negotiable Salary

Indeed

Dialysis Nurse (m/f)

Dialysis Nurse (m/f) \- Odivelas **Location:** Odivelas, PT, 2675\-624 **Date Posted:** 3 Nov 2025 **Contract type:** **Work Type:** On\-site **Part Time / Full Time:** Full Time **Visão:** For Life! To be the employer of choice in renal care **Missão:** Improve the quality of life of renal patients **Valores:** Competence, Passion, Inspiration **O que oferecemos:** * Our teams are made up of dedicated and skilled professionals who care and want to make a difference. * Our nurses represent the largest percentage of our employees. They are the professionals who build direct, lasting relationships and improve patients' quality of life every day. True experts in care, our nurses participate in cross-functional programs that promote personal development and idea exchange. * Our culture is based on the support we provide to patients, enabling them to live life to the fullest. We combine professional competence with a warm and human approach. **Responsabilidades:** * Provide nursing care in the different clinical care settings * Intervene based on the best scientific evidence, ensuring the implementation of quality standards; * Timely documentation of nursing interventions performed; * Promote patient autonomy, patient and family empowerment, and treatment adherence; * Communicate effectively with the patient and family; * Participate in and promote actions aimed at coordinating different levels of healthcare; * Actively participate in continuous improvement processes within their professional scope; * Report incidents; * Promote and participate in national or international research programs and projects; * Collaborate in the training and skill development process of other professionals; * Participate in the management and organization of the nursing team's work; * Solve clinical and organizational issues. **Requisitos:** * Bachelor's degree in Nursing and valid professional license * With or without experience in dialysis techniques * Proficiency in Portuguese and English * Knowledge of quality systems * Personal Skills: Initiative; Critical thinking; Decision making; Communication; Conflict management; Teamwork. **Benefícios:** * Integration into a young and dynamic team within a market-leading company * Access to initial and continuous training programs in dialysis techniques. Are you interested in being part of a team that is transforming renal care? Your trust is important to us! Want to know more about our data protection and privacy policy? Visit the information available at www.diaverum.com

Largo Dom Dinis 15B, 2675-368 Odivelas, Portugal

Negotiable Salary

Hemodialysis Nurse (m/f)640888591779861211

Indeed

Hemodialysis Nurse (m/f)

Hemodialysis Nurse (m/f) \- Lumiar **Location:**Lisbon, PT, 1750\-158 **Publication Date:** 18/09/2025 **Contract Type:****Job Type:** On-site **Part-Time/Full-Time:** Full-time Hemodialysis Nurse (m/f) \- Lumiar Diaverum provides renal care that improves the quality of life for people suffering from chronic kidney disease worldwide. Because everyone deserves a full life. Our experience in renal care dates back over 25 years, and we have been at the forefront of the industry ever since. Our operations currently span 24 countries, with more than 14\.000 motivated employees serving a patient base of over 40\.000 individuals. Find more information about Diaverum at www.diaverum.com . Grow with us! We are looking for a **Hemodialysis Nurse (M/F).** **Benefits:** Integration into a young and dynamic team within a market-leading company Access to initial and continuous training programs in dialysis techniques. **Requirements:** Bachelor's degree in Nursing and valid professional license Experience in dialysis techniques (preferred) Proficiency in Portuguese and English (preferred) Knowledge of quality management systems (preferred) Personal Skills: Initiative; Critical thinking; Decision making; Communication; Conflict management; Teamwork

Av. David Mourão-Ferreira 1750, 1750-314 Lisboa, Portugal

Negotiable Salary

Operating Room Nurse (m/f)642780402895391212

Indeed

Operating Room Nurse (m/f)

**In your daily activities, you will perform the following duties:** * Provide nursing care according to the surgical specialty within the perioperative and postoperative scope; * Welcome the patient and prepare them for surgery; * Participate in projects, training sessions, and events in accordance with the strategic and commercial policy of Grupo Trofa Saúde; * Use computer software for all essential nursing practice records; * Coordinate work with multidisciplinary teams; * Deliver appropriate nursing care tailored to different surgical specialties within the perioperative context; **What we value:** * Bachelor's or Master's degree in Nursing; * Minimum of 2 years of experience (preferred); * Hold a Professional Registration Certificate from the Portuguese Nurses Order; * Strong sense of responsibility; * Ability to work in a team and cooperate towards common goals; * Initiative and dynamism; * Availability to work shifts; * Proficiency in computer applications; **What we offer:** * Integration into a leading group in the private healthcare sector in Portugal; * Job stability; * Career progression opportunities; * Health insurance; * Commercial discounts with various partners.

PV49+C7 Lisbon, Portugal

Negotiable Salary

Clinical Research Associate, Multi-Sponsor - Based in Lisbon642124076807691213

Indeed

Clinical Research Associate, Multi-Sponsor - Based in Lisbon

**Clinical Research Associate** **Your responsibilities will include:** * Performing site selection, initiation, monitoring and close\-out visits * Supporting the development of a subject recruitment plan * Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines * Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions * Collaborating with experts at study sites and with client representatives **Qualifications:** * University degree in scientific discipline or health care * Requires at least 1 year of on\-site monitoring experience. * Very good computer skills including MS Office * Excellent command of Portuguese and English language. * Organizational, time management and problem\-solving skills * Ability to establish and maintain effective working relationships with coworkers, managers, and clients * Flexibility to travel * Driver’s license class B **What you can expect:** * Resources that promote your career growth * Leaders that support flexible work schedules * Programs to help you build your therapeutic knowledge * Excellent working environment in a stabile, international, reputable company * Company car, mobile phone and attractive benefits package IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi\-talented collaboration harnesses innovation to deliver superior outcomes. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi\-talented collaboration harnesses innovation to deliver superior outcomes.

R. António Sérgio 5, 2780-199 Oeiras, Portugal

Negotiable Salary

Contact Center Analyst – Italian Speaking642124077021451214

Indeed

Contact Center Analyst – Italian Speaking

**Contact Center Analyst – Italian Speaking** **Lisbon, Portugal** **Homebased/Remote** We are looking for a committed and technically skilled Contact Center Analyst who is fluent in Italian to become part of our team. This position is crucial for delivering initial support to Pharmaceutical Advisors, ensuring technical assistance services, and offering a first\-line support service for the Customer Relationship Management (CRM) System. The Analyst will provide email, phone, and remote technical support to customers to resolve issues related to product usage or system malfunctions. **What to expect:** * Deliver first\-line technical support and resources to both internal and external customers. * Engage with end users to clarify and define their requirements, ensuring a thorough understanding of their needs. * Resolve routine technical issues and escalate more complex problems to the appropriate support teams. * Maintain detailed call information in our database using commercial software. * Assist with configuration and installation of PC workstation hardware and software. * Update and complete the helpdesk knowledge database. **What we’re looking for:** * Fluency in Italian and professional English proficiency. * A college certificate or equivalent experience in IT, customer service, or related fields. * Experience in a Service Desk or IT Support environment. * Solid knowledge of Windows OS and Microsoft Office Suite. * Strong communication and problem\-solving skills. * A calm, logical approach under pressure and a collaborative mindset. **What you’ll receive:** * Comprehensive technical training and continuous learning opportunities. * A collaborative, multilingual team that values your input and growth. * Exposure to international clients and projects in the pharmaceutical sector. * Opportunities to grow your career within a global organization. **Why Join?** Those who join us become part of a recognized global leader still willing to challenge the status quo to improve patient care. You will have access to the most cutting\-edge technology, the largest data sets, the best analytics tools and, in our opinion, some of the finest minds in the Healthcare industry. You can drive your career at IQVIA and choose the path that best defines your development and success. With exposure across diverse geographies, capabilities, and vast therapeutic and information and technology areas, you can seek opportunities to change and grow without boundaries. We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. **It's an exciting time to join and reimagine what's possible in healthcare.** *IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential.* IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi\-talented collaboration harnesses innovation to deliver superior outcomes.

R. António Sérgio 5, 2780-199 Oeiras, Portugal

Negotiable Salary

Indeed

Business Analyst

**Join us on our exciting journey!** IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, Technology, analytics and human ingenuity to drive healthcare forward. **Job Description Summary** We are seeking a skilled Business Analyst with a strong foundation in business processes and computing technologies to support a strategic global initiative at IQVIA. This role involves close collaboration with business stakeholders, data experts, and development teams to ensure that project data, data models, and mappings are accurately documented and aligned with governance standards. The analyst will also coordinate with internal stakeholders to support the analysis, sourcing, and validation of new data assets to meet evolving project requirements. **Key Responsibilities:** Document data sources, data models, and metadata, including a comprehensive attribute inventory of current HCP, HCO, Scientific, and Digital data assets. Coordinate and contribute to the assessment of data gaps, data mapping, and the acquisition of new data sources in collaboration with internal stakeholders. Interpret, describe, convert, and map data from disparate or custom data models into standardized formats, ensuring consistency, accuracy, and traceability. Maintain and update data dictionaries, lineage documentation, and metadata repositories. Support data governance practices, including data quality management, ownership definition, and regulatory compliance. **Our Ideal Candidate Will Have:** Minimum of 3 years of relevant professional experience. Bachelor’s degree in Computer Science, Biotechnology/Healthcare, Business Administration, or a related field (or equivalent practical experience). Proven experience in data analysis, data mapping, and data warehousing. Strong technical background with experience working alongside software development teams. Foundational knowledge of programming languages (e.g., Python, SQL), database systems (e.g., Oracle, MongoDB), data engineering tools (e.g., ETL pipelines), and cloud platforms (e.g., AWS, Azure). Excellent analytical and documentation skills. Strong written and verbal communication skills, with the ability to clearly explain moderately complex healthcare data concepts to both technical and non\-technical audiences. Effective coordination and stakeholder engagement capabilities. Ability to work independently and thrive in a remote team environment. **Preferred:** Experience in the commercial pharmaceutical industry or healthcare analytics. Certification in project management (e.g., PMP, PRINCE2\) or business analysis (e.g., CBAP).**PLEASE SUBMIT YOUR CV IN ENGLISH \- APPLICANTS MUST HAVE THE RIGHT TO WORK IN THE COUNTRY THEY ARE APPLYING TO!** We know that meaningful results require not only the right approach but also **the right people**. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and **Whatever your career goals, we are here to ensure you get there!** **We invite you to join IQVIA™.** IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi\-talented collaboration harnesses innovation to deliver superior outcomes.

R. António Sérgio 5, 2780-199 Oeiras, Portugal

Negotiable Salary

Product Vigilance Expert642013481848341216

Indeed

Product Vigilance Expert

We are seeking a highly motivated and experienced Product Vigilance Expert to lead and manage product vigilance activities. This role ensures compliance with local regulations and global procedures for pharmacovigilance, cosmetovigilance, materiovigilance, and nutrivigilance. The successful candidate will serve as the primary point of contact for safety matters with local health authorities and oversee safety operations **Pharmacovigilance System Oversight** * Manage vendor resources across assigned territories. * Support the Area Safety Head with inputs for the EEA Pharmacovigilance System Master File. * Identify and investigate non\-conformances; implement CAPAs. **Safety Management \& Reporting** * Respond to safety\-related queries from health authorities. * Reconcile safety data with internal and external stakeholders. * Oversee literature screening for AE reporting. * Manage safety documentation and archiving. * Ensure LOC personnel are trained on safety reporting. * Monitor regulatory changes and notify authorities of safety issues. * Submit safety reports (SAE, SUE, SUSARs, PSUR, RMP). * Translate ICSR and PV documents as needed. **Collaboration \& Strategic Support** * Contribute to global and local safety projects and initiatives. **Procedural Documentation** * Develop and maintain local procedures aligned with global standards and national regulations. **Audit \& Inspection Readiness** * Support audits and inspections; respond to queries and implement CAPAs. **Vigilance Contract Management** * Manage vigilance clauses and contracts, including setup, revisions, and reconciliations. **Business Continuity** * Ensure local business continuity plans are in place, including AE reporting coverage and inspection readiness. **Education:** * Degree in a healthcare science discipline (e.g., Pharmacist, Nurse) **Experience:** * Minimum 3 years in the CRO/pharmaceutical industry with product vigilance responsibilities. **Skills \& Competencies:** * Strong organizational and workflow management skills * Proficient in safety\-related IT systems * Excellent communication skills (verbal and written) * Ability to build relationships with internal teams and health authorities * Deep understanding of local and global product safety regulations * **Native Spanish speaker;** fluent in English IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi\-talented collaboration harnesses innovation to deliver superior outcomes.

R. António Sérgio 5, 2780-199 Oeiras, Portugal

Negotiable Salary

Indeed

Nurse

Job Description The Nurse ensures the assessment and delivery of nursing care aimed at promoting, maintaining, and restoring residents' health, as well as preventing diseases and disabilities. **Main Functions and Responsibilities:** 1\) Accompany and attend to residents, meeting their general, human, and health needs, especially when they require nursing services. 2\) Prepare and administer medications according to clinical prescriptions, particularly treatments. 3\) Measure blood pressure, pulse, temperature, and weight. Perform glucose and oxygen saturation tests. Collect and record data. 4\) Collaborate with physicians by preparing materials and medications for use. 5\) In the physician's absence, inform residents and/or family members about the resident's health status. 6\) Organize clinical records and document all relevant data related to their duties. 7\) Provide care for bedridden residents due to illness, monitoring residents' feeding and directly feeding users requiring assistance (nasogastric tube, gastric tube, etc.). 8\) Supervise and support the execution of physical activities prescribed by the physician, observing any incidents that may occur during their implementation. 9\) Adhere to hygiene and dress code regulations. 10\) Follow quality standards and procedures. 11\) Actively participate in training programs provided by the company. 12\) Generally, perform all other unspecified tasks requested that are related to the above responsibilities. Profile The Nurse must hold a Bachelor's degree in Nursing and a valid registration with the professional board. We Offer Development opportunities within a rapidly expanding Group. Continuous training. Competitive salary.

Rua Padre Manuel Frango de Sousa 24, 2925 São Lourenço, Portugal

Negotiable Salary

Clinical Research Associate - based in Portugal640976510065941218

Indeed

Clinical Research Associate - based in Portugal

R. António Sérgio 5, 2780-199 Oeiras, Portugal

Negotiable Salary

Clinical Sales Representative640890893354271219

Indeed

Clinical Sales Representative

About the job Clinical Sales Specialist Zona Norte (Lisboa Porto) A **Elevus** is recruiting in the medical sector during a phase of expansion, integrating a **Clinical Sales Specialist** for the **Norte region (Lisboa Porto)**. This role will be responsible for driving business in the region, ensuring follow-up with hospital and clinical clients, and contributing to the sustainable growth of operations in Portugal. **Main Responsibilities** * Manage the complete sales cycle from prospecting to closing deals; * Promote technological and medical solutions to **hospitals, clinics and healthcare professionals**; * Maintain trustful and close relationships with customers; * Prepare commercial proposals and ensure after-sales support; * Identify business opportunities and gather market information. **Ideal Candidate Profile** * Bachelor's degree in **Business Administration, Biomedical Engineering or related field**; * **3 to 5 years of experience** in sales roles within the **medical, healthcare or medical devices sector**; * Strong network of contacts in the hospital market of the **Northern region**; * Fluent in **Portuguese and English** (French is a plus); * Autonomous, communicative profile with a results-driven mindset. **Offered Conditions** * **Competitive salary \+ performance bonus**; * **Company car, health insurance, mobile phone and laptop**; * **Hybrid/home office** arrangement, with monthly meetings in Lisbon; * Opportunity to join a **solid and rapidly growing project** in the medical sector. Type of offer: Full-time/Integral

PV49+C7 Lisbon, Portugal

Negotiable Salary

Indeed

Manual Tester

We are recruiting a **Manual Tester** (m/f) to strengthen our team with the possibility of working in a hybrid mode. **What we are looking for:** * Bachelor's degree in Computer Engineering, Biomedical Engineering or similar areas (preferable); * 4 years of experience (minimum) in manual testing; * Experience in web and mobile testing; * Experience with testing tools; * Must have the ability to analyze requirements, create/execute/manage test cases, test cycles and defect management; * Experience with Jira and Confluence; * Experience in agile methodologies; * ISTQB certification (an advantage). **What we offer:** * Work model flexibility (hybrid); * Regular follow-up plan; * Participation in projects with innovative technology and international scope; * Competitive salary based on demonstrated experience, health insurance and life insurance; * Birthday day off and referral bonus. If you identify yourself with this profile, send us your updated CV to recrutamento@movilges.com If you want to know more about Us: Movilges IT Consulting has over 30 years of experience in the Spanish market, specialized in Logistics, Mobility and IT, offering Consulting services, application development and system maintenance. Just like the technological universe, in constant evolution, Movilges IT Consulting also aims to grow, increasing its presence in Portugal, not only providing the best services to partners and clients but also offering the best conditions, benefits and professional growth opportunities for its entire team. In Portugal, we are present in different sectors such as technology, healthcare, public administration, energy, services, banking and insurance. By sending us your application, you authorize Movilges IT Consulting to process your personal data such as name, email, phone contact and information regarding your academic and professional experiences contained in your CV. The processing of this data serves only the legitimate purposes of the company, that is, for recruitment processes of qualified professionals for our team. For any questions regarding your personal data, you can contact us at portugal@movilges.com

PV49+C7 Lisbon, Portugal

Negotiable Salary

Business Analyst -Documents640890662499851221

Indeed

Business Analyst -Documents

**Date:** 6 Oct 2025 **Company:** Qualitest Group **Country/Region:** PT At **Qualitest** we're all about ensuring everything runs smoothly, whether it's your business, technology, or operations. We leverage smart engineering\-led practices and precise processes to maintain excellence in all that we do. **Our clients are the world’s top brands** and our diverse **global team of 8,000 employees** who collaborate with industry leaders in technology, finance, insurance, and beyond, making a significant impact in the world of technology. **Overview:** We are looking for an **IT Business Analyst based in Lisbon** whose primary focus will be to **design the requirements for the Documents and E\-mail templates** to be configured on the IT landscape that will support the business across Europe within a Transformation Programme **Requirements:** * Liaise between with the business to understand their requirement * Perform fields mapping for documents * Analytical and detailed perspective to identify gaps and perform requirement analysis * Document the requirements for the Documents/E\-mails in scope for each project/release and keep it updated * Support any queries from development team and testing phases **What are we looking for:** * At least 5 years of experience as a Business Analyst or Systems Analyst, working in an IT and/or technical environment is essential * Insurance business knowledge to understand business cases * Strong knowledge of business analysis tools and techniques, such as user stories, use cases, wireframes, UML, BPMN, etc * Experience in working with agile methodologies, such as Scrum and Kanban * Previous or current experience in testing would be an advantage * Excellent communication, presentation, and facilitation skills * Must be able to work independently and proactively in a fast\-paced and dynamic environment * Use of English as a working language (both written and spoken) * Experience in Atlassian tools (Confluence, JIRA, Trello) * Good / advanced Excel skills **What can we offer you:** * Hybrid model * Competitive salary * Meal allowance * Fixed term contract * Health Insurance * Psycological Support * Qualitest Allowance Ready to make a difference? Join our dynamic and forward\-thinking team!

PV49+C7 Lisbon, Portugal

Negotiable Salary

Indeed

CAR-T SFDC IT Analyst

At Johnson \& Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Technology Product \& Platform Management**Job Sub Function:** Business Systems Analysis**Job Category:** Scientific/Technology**All Job Posting Locations:** Breda, Netherlands, High Wycombe, Buckinghamshire, United Kingdom, Issy\-les\-Moulineaux, France, Lisbon, Portugal, Madrid, Spain, Milano, Italy**Job Description:** Are you having a first experience in SFDC, and having a passion for digital health solutions, enabling personalized treatment? Johnson \& Johnson is recruiting a **CAR\-T SFDC IT Analyst**, located in Europe. The EMEA Advanced Therapies Product Group is recruiting a CAR\-T SFDC IT Analyst. This role is responsible for translating the business needs into design specifications and user stories for the SFDC Health Cloud instance of the regional CAR\-T digital platform. The analyst will provide an optimal solution design and will follow\-up on the delivery within the squad. Our CAR\-T digital platform combines multiple off\-the\-shelf and custom\-built solutions to deliver a reliable and streamlined commercial experience for our customers across the patient \& cell journey. The platform is being rolled out throughout Europe and needs to support compliance to various requirements and support different delivery models. ### **Key Responsibilities:** * Understand user needs and translate them into detailed requirements for the SFDC Health Cloud solution squad * Collaborate across teams to build use cases; write, manage, and clarify user stories, visualization, and process flows. Drive and improve user experience. * Work with cross\-functional teams to solve complex challenges and ensure platform meets business needs. * Communicate with different stakeholders at different levels in the organization, follow\-up on the user stories with the developers and testers and manage dependencies with relevant squads * Support the creation of test scripts and participate in User Acceptance Testing as needed * Apply compliance requirements within scope of responsibility, ensure SDLC documentation, system configuration and compliance activities are up to date as required. ### **Qualifications** **Education:** * Master’s or bachelor’s degree and a minimum of 2 years of experience in the world of technology ### **Experience and Skills:** **Required:** * SFDC experience is required. Knowledge of SFDC Health Cloud is an asset. * Hands on knowledge in enhancing business processes with a focus on user experience * Strong problem\-solving skills with ability to accurately analyze situations and design solution proposals * Ability to work independently while staying aligned with team’s objectives. Excellent teamwork and collaboration in cross\-functional teams * End\-to\-end thinking and curiosity about the big picture * Passionate to stay up to date with current trends, best practices and new technologies **Preferred:** * SFDC certifications * Knowledge of system integration technologies (especially API) * Experience in Life Sciences or another regulated industry * Knowledge of Cell and/or Gene Therapy technologies is a nice\-to\-have **Other:** * Good communicator in English (written and spoken) * Up to 10% travel

PV49+C7 Lisbon, Portugal

Negotiable Salary

Integration Functional Test Analyst640890662269471223

Indeed

Integration Functional Test Analyst

**Date:** 6 Oct 2025 **Company:** Qualitest Group **Country/Region:** PT At **Qualitest** we're all about ensuring everything runs smoothly, whether it's your business, technology, or operations. We leverage smart engineering\-led practices and precise processes to maintain excellence in all that we do. **Our clients are the world’s top brands** and our diverse **global team of 8,000 employees** who collaborate with industry leaders in technology, finance, insurance, and beyond, making a significant impact in the world of technology. **Overview:** We are looking for a **Integration Functional Test Analyst,** **based in Lisbon,** whose primary focus will be to design and execute the test cases for the File integrations within the Integration Layer of our IT landscape the supports our insurance business across in Europe within a Transformation Programme. **Responsibilities:** * Support the Product Owner in constructing a backlog of test cases * Be an integral part of the squad and drive the quality of the file integrations in a timely manner * Consume and understand complex specifications and turn these into test cases and valid input / output data * Collaborate with engineers, testers, and other team members to ensure quality and timely delivery * Communicate effectively with all levels of stakeholders, both verbally and in writing **What are we looking for:** * Proven experience in handling File integration testing. Able to setup test cases and execute them, validating several input to expected output files (excel, csv, txt, xml, json) * ISTQB Foundation Certificate (concluded) * At least 3 years in functional testing * Knowledge in Agile Scrum and experience working in Agile scrum teams. * English B2 or above \- work language will be English. * Previous experience in insurance business is a plus, not mandatory **What can we offer you:** * Hybrid model * Competitive salary * Meal allowance * Fixed term contract * Health Insurance * Psycological Support * Qualitest Allowance Ready to make a difference? Join our dynamic and forward\-thinking team!

PV49+C7 Lisbon, Portugal

Negotiable Salary

Clinical Laboratory Technician640888592844811224

Indeed

Clinical Laboratory Technician

**Clinical Laboratory Technician** ================================== **Localização:** Centro Champalimaud **Entidade Empregadora:** Fundação Champalimaud **Regime:** Tempo Inteiro **Posição:** Técnico **Início da Candidatura:** 24 Set. 2025 The Cell Centre is looking to expand efforts in the GMP production of cell products with a specific focus on immune\-monitoring. The successful applicant is expected to be pivotal co\-worker in the development and improvement of immune cell\-based therapies for malignant diseases and the preparation of GMP compliant production of cellular products including gene\-modified immune cells and monitoring of anti\-cancer directed vaccination. Duties \& Responsibilities * Lab management and organisation with an excellent team and collaborative spirit within the institution and with our international partners; * Close interaction with clinical colleagues and within immunotherapeutic programs; * Analysis and interpretation of immune responses; * Procurement of clinical samples and subsequent processing for molecular and functional analysis; * Procurement of cellular products for (non\-vector and vector\-based) therapy; * Excellent expertise in in tissue culture; * Advanced flow cytometric analyses; * Excellent knowledge or dedication to acquire strong skills in QC documentation. Qualifications \& Skills * Strong knowledge in human T\-cell and B\-cell biology and immunology; * Documented and well advanced practical and theoretical knowledge in cellular analysis and immunological assays to gauge cellular and humoral immune responses; * Previous work experience with lentiviral (LV) and non\-LV based gene transfer is a plus; * Skills in DNA and RNA processing; * Very good knowledge in molecular technologies, excellent knowledge in flow cytometry, T\-cell sorting and gauging immune effector functions; * Team spirit and will to collaborate within the foundation and with our partner institutions with the possibility to travel for clinical, international projects; * Fluency in English and excellent communication skills (written and verbal) in English. Requirements * Research Field: Biological sciences » Other * Education Level: Master Degree or equivalent How to apply To apply, please send a letter of motivation, a 2\-page CV and the names and contact information of 2 references to markus.maeurer@fundacaochampalimaud.pt with **“Laboratory technician \[your last name]”** in the subject line. Position will remain open until filled. About Us Research is at the heart of the Champalimaud Centre for the Unknown, a modern research and clinical facility situated on the waterfront in Lisbon, Portugal. Champalimaud Research comprises a team of over 250 scientists from around the world with foci in neuroscience and cancer research with a strong development in the production of cell therapy products. English is the official language of the Centre. Lisbon’s sunny Atlantic\-Mediterranean climate, vibrant culture and high quality of life make this a great place to live and work.

PV49+C7 Lisbon, Portugal

Negotiable Salary

Sponsor Dedicated Clinical Trial Manager - Home based EMEA, Hebrew Speaker640888593048341225

Indeed

Sponsor Dedicated Clinical Trial Manager - Home based EMEA, Hebrew Speaker

**Description** Sponsor Dedicated Clinical Trial Manager \- Home based EMEA, Hebrew Speaker Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** **Fluency in Hebrew and Deep knowledge of Israeli clinical processes are essential requirements.** **Overview** The role will be accountable for overseeing and maintaining **country (Israel) deliverables** as part of the overall project plan. Manages and maintains accurate country level plans. Ensures **timely communication bidirectionally** between the global and local study team. Cluster focused stakeholder management. **Main Responsibilities** * Responsible for documented review for reports/issues written by the CRAs/Lead CRAs. * Drives recruitment at regional/country level * Responsible for local country vendor management and oversight (as applicable). * Drives data cleaning at regional/country level **Requirements** * **Hebrew fluency** * **Previous experience with Israeli sites** and knowledge of Israeli RA contacts and regulatory and Submissions processes * At least 3 years of previous experience as Clinical Trial Manager * **Background \& Expertise**: + Preferably with historical CRA or strong site\-level experience + Solid understanding of site operations and dynamics. * **Start\-Up Phase Experience**: + Involvement in site selection, feasibility assessments, timeline planning, and recruitment support. + Experience working with vendors during study setup. * **Conduct Phase Responsibilities**: + Ability to support the study team during audits, inspections, and query resolution. + Strong leadership skills to manage complex or challenging conversations. + Experience in Oncology field and across different study phases * **Local Knowledge \& Language**: + Deep understanding of local (Israeli) regulatory and ethics processes. + Fluency in Hebrew **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Roles within the Clinical Trial Management job family at the P22 level are responsible for overseeing the development, coordination, and implementation of Phase 1 clinical research studies at the organization's facilities. Individuals in these roles collaborate closely with the principal investigator, serve as liaisons between research subjects, client teams, investigators, and clinic operations teams, and meticulously plan logistics and resource usage. These roles require tracking study progress in alignment with project milestones, client deliverables, and budget, while ensuring compliance with applicable regulations globally and by region.Impact and ContributionRoles within the Clinical Trial Management job family at the P22 level significantly impact the success of clinical trials by ensuring that all aspects of the study are meticulously planned and executed. Individuals in these roles contribute to the design, implementation, and delivery of processes, programs, and policies, leveraging their in\-depth knowledge and skills within the professional discipline. By managing processes and potentially directing the work of lower\-level professionals, these roles ensure that clinical trials are conducted efficiently and effectively, ultimately contributing to the advancement of medical research and the development of new treatments.Core Focus•Overseeing the development and coordination of Phase 1 clinical research studies•Collaborating with principal investigators and serving as liaisons between various stakeholders•Planning logistics and resource usage for clinical trials•Tracking study progress in alignment with project milestones, client deliverables, and budget•Ensuring compliance with global and regional regulations•Contributing to the design, implementation, and delivery of processes, programs, and policies•Managing processes and potentially directing the work of lower\-level professionals

Av. João Crisóstomo 57, 1050-126 Lisboa, Portugal

Negotiable Salary

Business Analyst/Product Owner. Healthcare. Clinical data640888593237781226

Indeed

Business Analyst/Product Owner. Healthcare. Clinical data

**Product Owner/ Sr. Business Analyst** **Platform Engineering \& Clinical data, Trial data, clinical trials Phase 1\-3** We are looking for a skilled and proactive Product owner to support and lead a team of Engineers delivering scalable, cloud\-native solutions in the Healthcare domain. This role is focused on projects involving clinical trial data, requiring a deep understanding of Clinical trials (Phase 1\-3\) workflows, data standards, and compliance. The ideal candidate will have experience working with modern clinical platforms, cell therapy context including patient journey mapping, chain of identity/custody, and TRiSP processes; and the ability to bridge business needs with technical execution. Plus, will lead the product lifecycle and prioritization for the orchestration system and similar clinical trial and therapeutics systems. He will act as the bridge between stakeholders, engineering, QA, and end\-users (clinicians, coordinators). Responsible for value delivery aligned with cell therapy , drug development and testing , audit reporting, clinical data reporting workflows. **Requirements** * 7\+ years of experience as a Business Analyst or Product Owner working with healthcare clinical data. * Strong domain expertise in clinician\-side and trials side processes. * Understanding of HIPAA and best practices for managing PHI/PII in healthcare data environments. * Familiarity with FHIR, HL7, and healthcare data integration standards. * Experience developing detailed requirements documentation, data dictionaries, and system/process diagrams. **Nice\-to\-haves** * Hands\-on experience with data validation and profiling for large\-scale claims datasets. * Exposure to GCP , AWS, Azure, or and their native data services. * Familiarity with both trials and clinical data models and their integration * Experience with BI/reporting tools such as Power BI, Looker, or Tableau. * Bachelor’s or Master’s degree in Healthcare Informatics, Information Systems, or a related field. **Core Responsibilities** * Act as a liaison between business stakeholders and the Data Engineering team, translating complex clinical data requirements into actionable development tasks. * Lead discovery and requirements workshops focused on operations, data intake, chain of custody and other related processes. * Document end\-to\-end data flows, business logic, data mapping, and acceptance criteria for ingestion, transformation, and reporting of trial related data. * Own and maintain the product backlog, grooming epics and user stories. * Prioritize features based on patient journey insights and commercial scalability. * Engage with cross\-functional stakeholders (clinical ops, QA, regulatory, sites). * Drive agile ceremonies: sprint planning, reviews, retrospectives. * Translate regulatory and CoI/CoC needs into technical requirements. * Align product vision with roadmap and commercialization/ Research goals. * Define success KPIs (e.g., scheduling efficiency, alert accuracy). * Oversee user research, prototyping, and usability assessments. * Ensure integration with EMR, LIMS, EDC, and drug manufacturing , supply chain systems. * Track product progress and adjust roadmap based on feedback and pilots. * Design role\-based access control and user provisioning workflows. * Implement audit trail monitoring and exception logging. * Review and enforce HIPAA, GDPR, and 21 CFR Part 11 requirements. * Conduct security risk assessments and pen testing coordination. **Soft Skills** * Excellent communication skills, both written and verbal, with the ability to work across business and technical teams. * Strong problem\-solving skills and attention to data accuracy. * Self\-starter with the ability to lead initiatives with minimal oversight. * Passion for improving healthcare operations through better data and technology. **Why Join Us?** * Influence data\-driven decision making in healthcare with real\-world impact. * Work on modern cloud platforms (Google Cloud, Databricks/Snowflake, AWS, etc.). * Join a team of high\-performing engineers and healthcare data experts. * Thrive in a flexible, collaborative, and mission\-driven environment. **What we offer** * Continuous learning and career growth opportunities * Professional training and English/Spanish language classes * Comprehensive medical insurance * Mental health support * Specialized benefits program with compensation for fitness activities, hobbies, pet care, and more * Flexible working hours * Inclusive and supportive culture **About Us** Established in 2011, Trinetix is a dynamic tech service provider supporting enterprise clients around the world. Headquartered in Nashville, Tennessee, we have a global team of over 1,000 professionals and delivery centers across Europe, the United States, and Argentina. We partner with leading global brands, delivering innovative digital solutions across Fintech, Professional Services, Logistics, Healthcare, and Agriculture. Our operations are driven by a strong business vision, a people\-first culture, and a commitment to responsible growth. We actively give back to the community through various CSR activities and adhere to international principles for sustainable development and business ethics. To learn more about how we collect, process, and store your personal data, please review our Privacy Notice: https://www.trinetix.com/corporate\-policies/privacy\-notice

PV49+C7 Lisbon, Portugal

Negotiable Salary

Feasibility Study Specialist I640888592396811227

Indeed

Feasibility Study Specialist I

**Feasibility Study Specialist I** (Please note this role can be located in any country where CTI has a legal entity) **Job Purpose / Summary** Assists in analyzing and researching institutions and Investigators via CTI Feasibility Database, Data Assets and Business Intelligence to develop site, investigator and patient information for business development proposals and post\-award feasibility offerings. Responsibilities include assist with compiling feasibility reports, presentations, and sample site assessment for investigator feedback on study design and logistics, as well as enrollment potential, worldwide. This position reports directly to the Manager, Feasibility. **What You'll Do** * Research and compile information on therapeutic area(s), collect information regarding incidence, prevalence, standard of care, factors determining and influencing indication frequency and distribution, treatment trends, competing trials, etc. * Carry out database and literature search for sites identification * Assist in the identification/selection of potential sites and investigators and be able to present results to the internal team * Assist inthe design of initial interest emails, site surveys/questionnaires to obtain key information (e.g., investigator feedback on projected enrollment, feasibility of the study, and site capabilities); * Draft online survey (eg. Survey Monkey) based on the approved questionnaire to facilitate the collection of data in the most efficient manner. * Track responses of the online survey results and compile information for decision making. * Ensure that feasibility tracking (Initial interest, CDA, survey completion, Feasibility teleconferences) and status updates are completed in real time and organize the information for review with the internal team and external client. * Follow\-up with internal team, sponsor and/ or site staff regarding feasibility status * Enter information obtained into CTI feasibility data base in order to ensure that the database is up to date at all times * Assist in the preparation, as applicable, of the feasibility call script for each site feasibility teleconference in order to ensure that all relevant and critical information will be obtained – review script with manager for approval * Organize all aspects of the feasibility calls with the sites in order to ensure that these call run effectively Assist in the preparation of presentations and/or written reports, as required, by summarizing the relevant information and discussing within the team in order to present to sponsor and obtain next step approval. * Participates in intra\- and inter\-departmental meetings including kick off meetings as well as sponsor meetings. **What You'll Bring** * High School Graduate * 0\-1 years pharmaceutical or CRO Clinical Research experience * Excellent verbal and written communication skills * Excellent organizational, time and personal management skills * Good data analytic skills * Good creative problem\-solving skills * Creative skills and ability to think outside the box * Ability to maintain confidentiality * Ability to multitask to tight timelines prioritizing workload and maintaining high quality standards * Proficiency in use of computer and software systems * Ability to understand, interpret, and explain complex regulatory requirements and details * Fluent in spoken and written English **Why CTI?** * We support career progression – 25% of our global staff is promoted annually and we have a structured mentoring program to provide the support you need to move forward * We value education and training – We provide tuition reimbursement, partner with universities and colleges to create programs in our field, and have a dedicated training department * We value our people \- We have never had a layoff in our 20\-year history, support a work\-life balance with flexible schedules, and have provided cash bonuses every year for the past decade * Our culture is unparalleled – Click here to learn more about “The CTI Way” * We think globally and act locally – We have a global philanthropic program supporting our team’s efforts to improve their local communities (Click here to learn more about our “CTI Cares” program) * We are looking toward the future – We have had a consistent 15% growth rate over the last decade, invest in cutting\-edge technology, and pride ourselves on our average 95% annual retention rate * Our work makes a difference – We focus our work on treatments for chronically and critically\-ill patients, who are depending on us to bring these life\-changing therapies to market

R. Infantaria 16 60, 1350-168 Lisboa, Portugal

Negotiable Salary

Research Technician - Cancer and Stem Cell Biology Lab640888592618271228

Indeed

Research Technician - Cancer and Stem Cell Biology Lab

**Research Technician \- Cancer and Stem Cell Biology Lab** =========================================================== **Localização:** Champalimaud Centre for The Unknown **Entidade Empregadora:** Champalimaud Foundation **Regime:** Tempo Inteiro **Posição:** Research Técnico de Investigação **Início da Candidatura:** 01 Out. 2025 Offer Description Champalimaud Foundation (Fundação D. Anna de Sommer Champalimaud e Dr. Carlos Montez Champalimaud), a private, non\-profit research institution in Lisbon, Portugal, is looking for a **Research technician** to join our team at the Champalimaud Research Program. The selected candidate will participate in running in vivo and in vitro experiments aimed at studying the mechanisms involved in cancer formation. This position will include a broad and evolving range of tasks, including: * Genotyping mice; * DNA extraction, primer design, PCR, gels; * Colony management; * Mice handling and treatment; * Designing and keeping track of the breedings, weaning and cage use; * Immunohistochemistry and immunofluorescent stainings; * Cell culture; * Lab orders. Requirements Research Field: Biological sciences Education Level: Master Degree or equivalent ***Skills/Qualifications*** Minimum qualifications: Master in Science ***Specific Requirements*** ***Essential skills*** * Ability to work independently on defined day\-to\-day research tasks * Experimental research experience * Experience handling and treating mouse models of cancer * Knowledge on genetic mouse models of cancer * Good capacity for team work, critical thinking and communication skills * High level organisational skills * Ability to conduct research with honesty, accountability, professional courtesy and good stewardship in line with the Singapore Statement on Research Integrity *Desirable skills that will also be considered:* * Knowledge of PYRAT animal facility software * Experience in optimising PCR protocols for mouse genotyping * Interest in cancer and immunology Languages ENGLISH Level: Excellent Additional Information Benefits Competitive remuneration package commensurate with skills, qualifications and experience. Full immersion into a research excellence ecosystem with highly motivated researchers, supported by state\-of\-the\-art technology and continuous development opportunities. Maximum allowable duration of the contract: 12 months with possibility of renewal Eligibility criteria National, Foreign or Stateless candidate(s) who hold a master degree in Biology and Biotechnology and, Health\-related areas or other related scientific areas and a scientific and professional curriculum that reveals a profile appropriate to the activity to be developed. In case of PhD degrees awarded by foreign higher education institutions, the degree must comply with the provisions of Decree\-Law No. 341/2007, of 12th of October, and all formalities established therein must be fulfilled by the deadline for application submission. Selection process Candidates will be screened to determine eligibility based on minimum qualifications listed in call. Candidates meeting minimum requirements will be scored according to the required application materials: CV 70% weighting, motivation letter 20%, interview 10% (in case of a tie). If provided, and if shortlisted, candidates’ referees may be contacted and may count towards evaluation. Evaluation Committee members: Adriana Sánchez\-Danés and Patrícia Borges Application materials: CV and letter of motivation indicating 1 reference (one single pdf document). Proof of qualifications (certificates). Degrees obtained abroad may need to be formally recognised in Portugal. How to apply: Candidates must complete the standard application form and submit a single annexed PDF document containing the application materials stated in the call. The call reference will be asked and not having may invalidate your submission. This call reference is: "**RT Sánchez\-Danés Oct 2025**" Applications are also accepted in paper, sent or handed to the Fellows Support Office at the Champalimaud Centre for the Unknown, Avenida Brasília, 1400\-038 Lisbon, Portugal. Notification of results All candidates will receive a receipt of acknowledgment within 7\-10 business days. The highest scoring candidate will be notified by email or telephone. All other candidates will be notified solely by email of the final outcome of the recruitment process. After being notified, candidates will have 10 working days to present a claim for redress by email (careers@research.fchampalimaud.org). If no claim is received by the Champalimaud Foundation, the Evaluation Committee's decision will become definitive. About Us Research is at the heart of the Champalimaud Centre for the Unknown, a modern research and clinical facility situated on the waterfront in Lisbon, Portugal. The goal of Champalimaud Research (CR) is to perform world\-leading fundamental and translational research. Current research work is focused on the fields of neuroscience, physiology and cancer. Champalimaud Research comprises a team of over 400 scientists from around the world. English is the official language of the Centre. Lisbon’s sunny Atlantic Mediterranean climate, vibrant culture and high quality of life make this a great place to live and work. Relevant Institutional Information In line with our community guidelines and Equality, Diversity and Inclusion policy and Gender Equality Plan, no candidate may be privileged, favoured, prejudiced or deprived of any right or excluded from any duty on the basis of age, sex, gender identity, sexual orientation, race/ethnicity, disability, chronic illness, language, nationality, territory of origin, family status (marital, pregnancy and maternity, having or not having dependents), socioeconomic situation, education, religion, political or ideological beliefs, trade union membership, or on any other grounds which are irrelevant to decision\-making. Legal Notices The present call has the sole purpose of filling the indicated research position. This call may be canceled at any time on or before the jury’s evaluation of all eligible candidates and the recruitment process shall be concluded on the day of the full execution of the contract between the Champalimaud Foundation and the selected candidate.

PV49+C7 Lisbon, Portugal

Negotiable Salary

Indeed

Nurse (M/F) - Lisbon

Fisiolar, a specialist in providing home healthcare services, operates with excellence and professionalism in its services. Currently, Fisiolar is reinforcing its team of **Nurses** in the municipality of **Lisbon**. **\*ONLY APPLICATIONS SUBMITTED THROUGH THE LINK WILL BE CONSIDERED: https://smartfisiolar.bitrix24\.site/candidatura/** Our collaborators represent our identity, therefore our prerequisites include: \- Bachelor's or Master's degree; \- Portuguese Professional License; \- Professional experience and specific training in different intervention areas (Preferred); \- Experience in Otorhinolaryngology (Preferred); \- Values such as respect for others, friendliness, professionalism, and proactivity are essential. Conditions: \- Work regime under service provision contract; \- Flexible working hours compatible with other professional activity(ies); \- Honorarium commensurate with the role. CONFIDENTIALITY: We guarantee the security and confidentiality of your data. The information provided allows us only to consider your application for potential future collaboration. The data used will not be used for commercial purposes. At any time, applicants may access their personal data, request rectification if inaccurate, request restriction of processing, deletion of data, exercise their right to object, or the right to data portability, under legally applicable conditions and according to current data protection regulations, by directing their request to our e\-mail. Offer type: Part\-time Benefits: * Flexible schedule Educational qualifications: * Higher education (Preferred)

PV49+C7 Lisbon, Portugal

Negotiable Salary