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Freelance Clinical Research Associate, CRA
ImmaticsFreelance Clinical Research Associate supporting clinical trials across Germany with focus on Source Data Verification. Engaging in clinical site management with interdisciplinary teams.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical trial site management, on-site monitoring, and regulatory compliance, with a strong focus on ICH-GCP standards and experience in oncology trials. Proficient in utilizing clinical trial systems such as eTMF, CTMS, EDC, and IRT while effectively communicating in both German and English.
Highest-signal resume keywords
Clinical Research Associate ExperienceOn-Site MonitoringSource Data VerificationICH-GCP KnowledgeClinical Trial Systems Familiarity
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial ManagementPatient Recruitment Progress ReviewTrial Master File ManagementData CaptureRegulatory Compliance
Soft Skills
Excellent Communication Skills
Tools & Technologies
ETMFCTMSEDCIRT
Industry Keywords
PharmaceuticalBiotechnologyCROOncology Clinical Trials
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- 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
What you’ll need- 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
Comp & perks- Flexible work arrangements
- Professional development opportunities