Clinical Research Associate (CRA) – Home Based – Germany
Locations: Düsseldorf, Essen, Münster, Bielefeld, Hannover, Erfurt, Nuremberg, Frankfurt am Main
Start: ASAP | Duration: 6 months | 0.8 FTE
About the Role:
We are seeking an experienced Clinical Research Associate (CRA) to join a leading global CRO supporting clinical trials across multiple therapeutic areas. In this role, you will coordinate and monitor clinical sites to ensure compliance with ICH GCP, FDA guidelines, local regulations, and standard operating procedures. You’ll work closely with investigational sites and project teams, supporting data quality, regulatory adherence, and successful trial execution.
Key Responsibilities:
- Conduct site visits to assess protocol adherence and regulatory compliance
- Manage clinical documentation to ensure audit readiness
- Provide mentorship and training to junior clinical team members
- Support project teams and take a lead role where required
- Collaborate with site staff and cross-functional teams to ensure smooth study operations
Requirements:
- University degree in a science-related field, healthcare professional certification, or equivalent
- 5 years of clinical research monitoring experience
- Fluent in English and local language (German)
- Valid driver’s license
- Expert knowledge of GCP, FDA guidelines, and clinical monitoring best practices
- Strong organizational, communication, and interpersonal skills
- Willingness to travel 60–80%
What We Offer:
- Flexible, home-based working arrangement
- Exposure to global clinical trials and diverse therapeutic areas
- Competitive hourly rate
- Opportunity to grow your expertise within a collaborative and supportive team
