Clinical Research Associate II – Regionalized Galicia - Maternity Leave Cover

Fortrea's FSP team is currently seeking two CRA II professionals to join the team in Galicia.

Summary of Responsibilities:

- Clinical site monitoring: conducts routine, pre‑study, initiation, and close‑out visits, ensuring full compliance with project plans.

- Site and patient protection: ensures informed consent, protocol adherence, and regulatory compliance to safeguard study participants.

- Data quality oversight: performs source document verification, CRF review, and manages data queries to ensure accuracy and completeness.

- Operational site management: prepares trip reports, ensures audit readiness, manages study files, coordinates with vendors, and uses resources efficiently.

- Safety reporting: tracks and follows up on Serious Adverse Events (SAEs), supporting report and narrative preparation.

- Extended support activities: feasibility assessments, QC visits, EC submissions, budget support, training/mentoring of new staff, and local project coordination.

- Cross‑functional communication & logistics: liaises with internal teams, manages study materials, and travels as required.

Qualifications (Minimum Required):

- University Degree in Scientific / Medical Field

- Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements in Spain

- Fluent in Spanish and in English, both written and verbal.

Experience (Minimum Required):

- Minimum 2 years of experience as independent monitor, working specifically within oncology: Prostate and Bladder cancer .

- Basic understanding of Regulatory Guidelines.

- Ability to work within a project team.

- Good planning, organization, and problem-solving skills.

- Good computer skills with good working knowledge of a range of computer packages.

- Valid Driver's License

Learn more about our EEO & Accommodations request here .