We are looking for anexperienced freelance Clinical Research Associate (CRA)to strengthen our client's project Team near Frankfurt am Main. Your expertise inmonitoring clinical research projectsacrossPhases I-IVis 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