Unblinded CRA in Germany

Join a sponsor-dedicated model supporting cutting-edge clinical trials in Germany. As an unblinded Clinical Research As sociate , you will contribute to high-quality clinical research delivery while gaining strong exposure to unblinded study activities in a collaborative global environment.

Key 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 audit readiness and ensure inspection preparedness at site level

Required 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 programs Flexible working model supporting work-life balance Access to global career growth opportunities within clinical operations Inclusive and collaborative culture with employee resource groups and wellbeing initiatives

If you are looking to build your clinical monitoring career within a high-impact and supportive environment, we encourage you to apply and grow with us.

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Learn more about our EEO & Accommodations request here .