other
Posted 1 weeks agoUnblinded CRA I based in Frankfurt or Ruhr Area
at Fortrea
Munich, GermanyRemote
Requirements
- Responsibilities You will perform unblinded monitoring activities in line with ICH-GCP guidelines and applicable regulations, including Investigational Product oversight You will ensure protocol compliance, data integrity, and patient safety at assigned sites You will maintain accurate and complete study documentation, including eTMF and regulatory files You will build strong relationships with site staff, acting as the primary point of contact for site management (pharmacy only) You could contribute to
- Qualifications Bachelor’s degree in Life Sciences or related field (or equivalent experience) Initial
- experience in clinical research as a CRA with at least 1 year of monitoring
- experience Understanding of ICH-GCP guidelines and clinical trial processes Strong interest and knowledge in unblinded study conduct and Investigational Product management Fluency in German and English (written and spoken) Willingness to travel within the Ruhrgebiet or Frankfurt region and across Germany as required Strong organizational skills with attention to detail What We Offer Opportunity to work in a sponsor-dedicated environment on innovative studies Structured onboarding and continuous development
Additional details
- Join a sponsor-dedicated model supporting cutting-edge clinical trials in Germany.
- As a Clinical Research Associate I or Clinical Research Associate II, you will contribute to high-quality clinical research delivery while gaining strong exposure to unblinded study activities in a collaborative global environment. Key
- #LI-GQ1 #LI-Remote Learn more about our EEO & Accommodations request here .