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.

📌 Clinical Research Associate II – Regionalized Galicia (Madrid)
🏢 Fortrea
📍 Madrid