CRA II: Clinical Trial Monitoring

PSI CRO is seeking a Clinical Research Associate II for a contract-based, home-based freelance position in Portugal. You will monitor sites, support startup, review CRFs, manage communications, and ensure data quality across multiple studies. The role requires strong English/Portuguese skills and willingness to travel. Ideal candidates have at least 1 year...

Fortrea Portugal seeks an experienced Clinical Monitor to oversee site management and monitoring activities for oncology studies in the Lisbon area. You will ensure ICH-GCP compliance, verify informed consent, perform source data verification, and maintain audit readiness while collaborating with global teams. Candidates should have at least 2 years...

Biostatistician II (Clinical Trial Experience Required) Requisition Number : BIOST Posted : October 9, 2026 Full-Time Hybrid Locations Showing 1 location Lisboa, Portgual Description What You'll Do: As the lead Biostatistician on the studies assigned, perform the following tasks: Act as primary statistical contact for internal and external project team...

Biostatistician II (Clinical Trial Experience Required) Requisition Number: BIOST002082 - Posted : October 9, 2026 - Full-Time - Hybrid Locations Showing 1 location Lisboa, Portgual Description What You'll Do: - As the lead Biostatistician on the studies assigned, perform the following tasks: - Act as primary statistical contact for internal and...

What You’ll Do: - As the lead Biostatistician on the studies assigned, perform the following tasks: - Act as primary statistical contact for internal and external project team members. - Communicate and work with Biostatistics management to maintain the project budget and timelines. - Review case report forms (CRFs) and completion instructions - Give...

ICON Strategic Solutions in Lisbon seeks a CRA II to design and analyze clinical trials, interpreting complex medical data and advancing treatments benefiting patients worldwide. The role involves site visits, protocol compliance, data integrity, and collaboration with investigators, with travel about 60% and a fast-paced environment. A science/healthcare...

IQVIA is seeking a Clinical Research Associate to support site selection, initiation, monitoring and close-out visits across studies. The role involves ensuring regulatory compliance and data integrity while coordinating with study sites and client representatives. The successful candidate will have a university degree in a scientific field or health care,...

Psi CRO is seeking a Contract Clinical Research Associate II to coordinate frontline communication with project stakeholders, ensure timelines, targets and data quality across various therapeutic indications, and maintain strong relationships with clinical sites and investigators. This home-based (freelance) role in Portugal requires at least 1 year of...

ICON Strategic Solutions is seeking an experienced Clinical Research Associate II to support sponsor-dedicated trials, designing and analyzing clinical data and contributing to trial monitoring to advance treatments for patients worldwide. You will conduct site visits, ensure protocol adherence, data integrity, and patient safety, collaborating with...