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Alimentiv 2

Sr. Clinical Research Associate (Germany)

Berlin · Munich · Frankfurt · Cologne · Dusseldorf · Hamburg · Stuttgart

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hirly's read of this role

Role family
Healthcare
Seniority
Senior
Country
DE
Work mode
Remote-friendly
First seen by hirly
18 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

Independently performs, coordinates and oversees all aspects of the clinical site monitoring services, assessing protocol and regulatory compliance as per Alimentiv’s and sponsor’s standard processes, ICH/GCP guidelines and local regulation. Serves as the primary liaison between the sponsor/Alimentiv and investigative sites by playing a critical role in the execution of clinical study plans. Provides guidance and mentoring CRA I and II, collaborating effectively with cross-functional stakeholders in a dynamic, results-driven and high-accountability environment. Perform CRA Assessment Visits and participate in audits/inspections, when required.

Original posting on Alimentiv 2's site ↗

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