Empregos de clinical research associate em Porto

Location Porto area preferred. Candidates based in Lisbon can also be considered.Are you passionate about clinical research and improving patients' lives? Do you thrive in a fast‐paced environment where quality, agility and collaboration matter? If you want to be part of a team delivering clinical trials that make a real difference, this could be your next...

Alimentiv is a global CRO with a singular focus: advancing therapies for patients with gastrointestinal diseases. GI is our WHY and for more than 30 years that purpose has driven our scientific rigour, operational excellence, and deep therapeutic expertise, including supporting more than 70% of IBD compounds in development. We operate as a private,...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a Freelance Senior Clinical Research...

Thermo Fisher Scientific in Portugal is seeking a Clinical Research Associate (Level II) to oversee site monitoring and regulatory compliance across global trials. You will conduct remote or on-site visits, manage essential documents, and ensure data integrity in line with ICH-GCP and sponsor SOPs. The role emphasizes risk-based monitoring, collaboration...

IQVIA in Lisbon, Portugal is seeking a Clinical Research Associate 2 to join our on-site team. You will perform site visits, support recruitment planning, and ensure compliance with ICH-GCP guidelines while coordinating with study sites and client representatives. The role requires a university degree in a scientific field, 2–4 years on-site monitoring...

A global clinical research provider is seeking a Clinical Research Associate 2 based in Portugal. The role involves performing site selection and monitoring visits, supporting subject recruitment, and ensuring regulatory compliance. Candidates must have a relevant university degree and a minimum of two to four years' experience in monitoring. Excellent...

Responsible for end-to-end site management and monitoring activities in clinical trials, ensuring compliance with GCP and protocol requirements, and serving as the primary liaison between the company and clinical sites.

As a Contract Clinical Research Associate II, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety...

Join an exciting oncology study and use your clinical research expertise to support accurate data management and successful trial delivery. R&D Partners is seeking a Clinical Research Coordinator for a part-time freelance role in Portugal. This is an exciting opportunity to contribute to oncology clinical research in the healthcare sector. The role requires...

Fortrea Development Ltd Sucursal em Portugal is seeking an experienced Clinical Monitoring professional to oversee site activities for oncology trials in Portugal. You will ensure adherence to ICH GCP, manage site training records, and perform end-to-end monitoring visits from initiation to close-out. The role requires 2+ years of independent monitoring...

Upsilon Global are seeking a Clinical Research Associate on behalf of an established mid-sized CRO to join their clinical operations team in Portugal. This CRO has developed a reputation as a leading employer within the clinical operations space, fostering growth opportunities and career progression through a variety of pathways and personal development...

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Clinical Site Payment Associate Manager based in Portugal. As a Clinical Site Payment Associate Manager, you will play a key role in managing clinical trial site payments, ensuring financial accuracy, regulatory compliance, and...

A leading investment management firm is seeking an Associate Analyst to conduct research and financial modeling on securities. The role offers a fully remote setup, flexible hours, and competitive compensation without bureaucracy. Ideal candidates will have strong analytical skills, 2-5 years of relevant experience, and be university graduates. This position...

Alimentiv is seeking an experienced CRA to independently perform site monitoring, coordinate visits and ensure protocol compliance in Portugal and Spain. You will mentor junior CRAs, collaborate with cross-functional teams, and participate in audits and inspections as needed. The role is home-based with regular travel (40-60%). A health sciences degree...

About the Company Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20 pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end‑to‑end clinical trial solutions across all phases, offering Phase I-IV...

Oncology Clinical Researcher (AI Training) About The Role What if your deep expertise in cancer clinical trials could directly shape how AI understands and reasons about oncology — influencing research that may one day save millions of lives? We're looking for experienced Oncology Clinical Researchers to bring real-world clinical rigor into cutting-edge AI...

Clinical Systems Analyst (AI Training) About The Role At Alignerr, we partner with the world's leading AI research teams and labs to build and train cutting-edge AI models. We're looking for experienced Clinical Systems Analysts to bring their real-world healthcare IT knowledge to AI development - helping ensure AI systems understand, reason about, and...

IQVIA is seeking a full-time Clinical Research Associate (CRA) in Porto Salvo, Portugal. The role covers site initiation, monitoring and close-out visits, plus supporting subject recruitment planning and regulatory compliance per GCP/ICH guidelines. You will track regulatory submissions, recruitment, CRF completion and data query resolutions while...

Alignerr Corp. is seeking a Principal Clinical Scientist to shape AI training using regulatory-grade clinical data. This fully remote, hourly-contract role demands senior expertise in trial design and regulatory science to ensure AI systems are built on scientifically sound data for biomedical research. You will design protocols, audit results, and evaluate...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a Clinical Database Programming Process...