Clinical Research Associate / Clinical Monitor / Site Manager | Biologe (m/w/d)
Alcedis GmbH
Job Summary
This role is for a Clinical Research Associate / Clinical Monitor / Site Manager who will be instrumental in overseeing and ensuring quality standards in healthcare centers and successfully planning and executing clinical drug trials (Phases I-IV), non-interventional studies, and medical device studies. The ideal candidate will support study organization, prepare and conduct monitoring visits (on-site or remote), validate study data, and ensure compliance with guidelines and laws. This position requires independent work, strong communication, and a proactive approach, with a focus on the North Rhine-Westphalia and West Lower Saxony regions, involving regular travel and quarterly visits to Gießen for team integration. It's an attractive opportunity for someone passionate about contributing to clinical research in a modern, supportive environment.
Required Skills
Education
University degree in Natural Sciences or Life Sciences, or Study Nurse qualification or equivalent
Experience
- • Professional experience in conducting GCP-compliant clinical studies within the industry (e.g., CRO, Pharma, or Biotech) is desirable
Languages
Additional
- Travel readiness (approx. 40-50% travel activity); Flexibility; Home-based contract combined with regular travel; Quarterly visits to Gießen (Hessen) for 1-2 days
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