Clinical Research Associate
vor 1 Tag
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.
Projektbeschreibung
- 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)
Skills
- 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
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