Freelance Clinical Research Associate, CRA

Immatics

Freelance Clinical Research Associate supporting clinical trials across Germany with focus on Source Data Verification. Engaging in clinical site management with interdisciplinary teams.

Posted 7/3/2026contractRemote • 🇩🇪 GermanyJuniorMid-LevelWebsite

Tech Stack

Tools & technologies

Google 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

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

Clinical Trial ManagementPatient Recruitment Progress ReviewTrial Master File ManagementData CaptureRegulatory Compliance

Soft Skills

Excellent Communication Skills