Jobbeschreibung
We are looking for an experienced freelance Clinical Research Associate (CRA) to strengthen our client's project Team near Frankfurt am Main. Your expertise in monitoring clinical research projects across Phases I-IV is crucial for overseeing and ensuring the quality of clinical trials. Your expertise is in demand! Apply now.
- Conducting On-site/Remote Initiation, Monitoring, and Close-out Visits
- Ensuring compliance with trial protocol, GCP, and regulatory requirements
- Performing Source Data Verification (SDV) (CRF vs. source patient data)
- Generating precise site visit and communication reports
- Diligent documentation in the Trial Master File (TMF)
- Close collaboration, training, and clarification with Investigators/site personnel
- Identifying and resolving deviations, discrepancies, and errors (Query Management)
- Degree in Life Sciences, Medicine, Pharmacy, or comparable
- Proven professional experience as a Clinical Research Associate (CRA) (Pharma/Biotech)
- Comprehensive knowledge of GCP, ICH Guidelines, and national laws
- Strong analytical and detail-oriented work approach
- Excellent communication and organizational skills
- Attractive options for shortening your personal payment term
- No more time-consuming invoicing
- Fast, reliable payment of fees
- Conclude project contracts by means of electronic signature