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

Planet Pharma

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Clinical Research Associate