Senior Clinical Research Associate - CNS - Immunology - Germany
Worldwide Clinical Trials · Posted Nov 6, 2026
- Remote, Germany
- Remote
- Senior
- 3+ years
Responsibilities
- Lead site qualification, initiation, interim monitoring, management, and close-out activities in accordance with study protocols, GCP, applicable regulations, and SOPs.
- Protect patient safety and data quality by reviewing informed consent, source documentation, CRFs, safety information, and protocol compliance.
- Partner with investigative sites to resolve data queries, maintain regulatory and site documentation, manage investigational product accountability, and support timely, accurate study data.
- Coordinate site regulatory and ethics documentation, study materials, and relevant documentation for the Trial Master File.
- Serve as a Lead CRA on global studies when required, coordinating CRAs and contributing to monitoring plans, study-specific tools, templates, and visit report reviews.
Requirements
- MD
- Pharmacy qualification
- four-year college qualification in a medical, biological, physical, health, pharmacy, or related science
- two-year college qualification or equivalent education/training, preferably in nursing or life sciences
- Nice to have: full-service monitoring