Fortrea seeks two Clinical Research Associates II for a maternity leave cover role in Galicia, Spain. The position involves site monitoring, data quality oversight, regulatory compliance, and safety reporting for oncology studies. Candidates must have a scientific/medical degree, minimum 2 years of independent monitoring experience in prostate and bladder cancer, and fluency in Spanish and English.

Responsibilities

- Conduct routine, pre-study, initiation, and close-out site visits with compliance verification
- Verify source documents, review case report forms, and manage data quality queries
- Track and follow up on serious adverse events and support report preparation
- Ensure informed consent, protocol adherence, and regulatory compliance at study sites
- Prepare trip reports,



maintain study files, manage materials, and coordinate with vendors

Requirements

- University degree in scientific or medical field
- Minimum 2 years experience as independent monitor in oncology (prostate/bladder cancer)
- Fluent in Spanish and English, written and verbal
- Thorough knowledge of ICH GCP guidelines and Spanish regulatory requirements
- Valid driver's license and reliable transportation
- Proficiency with multiple computer packages and software systems
- Strong planning, organization, and problem-solving abilities

📌 Clinical Research Associate II (España)
🏢 Fortrea
📍 España