Freelance Clinical Research Associate, CRA
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Job Description
Freelance Clinical Research Associate supporting clinical trials across Germany with focus on Source Data Verification. Engaging in clinical site management with interdisciplinary teams.
Responsibilities:
- Support clinical trial site management and monitoring activities
- Perform and support on-site monitoring visits
- Support the maintenance and updating of trial-specific tracking tools
- Collect site-specific clinical trial documents
- Support Trial Master File filing activities and TMF completeness checks
- Contribute to clinical trial site management and engagement
- Review patient recruitment progress and clinical data capture
Requirements:
- Degree in life sciences, nursing, medicine, pharmacy, or comparable field
- Solid experience as a Clinical Research Associate in pharmaceutical, biotechnology, or CRO environment
- Experience in on-site monitoring and Source Data Verification
- In-depth knowledge of ICH-GCP and applicable regulatory requirements
- Familiarity with clinical trial systems such as eTMF, CTMS, EDC, and IRT
- Experience in oncology clinical trials preferred
- Excellent communication skills in German and English
- Willingness to travel regularly within Germany
Benefits:
- Flexible work arrangements
- Professional development opportunities
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