Clinical Research Associate II – FSP Team, Galicia Area
This role supports clinical trials in oncology, hematology, and immunology across Spain, with a focus on maintaining study integrity and participant safety. The position is fully remote but requires residency in Galicia, preferably in Santiago de Compostela or La Coruña.
Key Responsibilities
- Perform routine monitoring activities, including pre-study, initiation, routine, and close-out visits to ensure adherence to protocols and timelines.
- Verify source documents and case report forms to support accurate and complete data collection.
- Ensure informed consent processes are properly documented and followed, and that regulatory requirements are met at all stages.
- Track and follow up on Serious Adverse Events, contributing to safety reporting and narrative development.
- Prepare detailed monitoring reports, maintain study files, and support audit readiness.
- Conduct feasibility assessments, quality control visits, and ethics committee submissions as needed.
- Collaborate with internal teams, manage study supplies, and coordinate logistics for site support.
- Assist in training and mentoring new team members and support local project coordination efforts.
Qualifications
- Master’s degree in a healthcare-related field or equivalent discipline.
- At least two years of experience in clinical monitoring or a related role.
- Familiarity with clinical trial regulations and good clinical practice guidelines.
- Proficiency in English and Spanish, both written and spoken.
- Strong computer literacy with experience in common software applications.
Work Environment
This is a fully remote position with a requirement to be based in Galicia. The role involves occasional travel to study sites. The team emphasizes collaboration, professional growth, and meaningful contributions to clinical research. Support for employee development is a core focus, fostering a supportive and forward-looking workplace culture.
