Clinical Research Coordinator I (m/w/d) - Deutschland
Core
Conduct and manage clinical trials in accordance with protocols, GCP, and SOPs, including patient recruitment, data management, and site visits.
Role type
Clinical Research Coordinator
Builds
Clinical trials for sponsors and CROs
Domain
Life Sciences / Clinical Research
Required skills
Medical terminology, GCP/ICH guidelines knowledge, Regulatory document preparation, Patient recruitment, Data entry and query resolution, Clinical procedures (medication prep, Fibroscan, Phlebotomy, EKG, lab processing), Protocol implementation, Site management
Preferred skills
Digital tools proficiency, Multitasking, Strategic decision making, Cultural diversity awareness
Technologies
Electronic Data Capture systems, Clinical trial management software
Responsibilities
Conduct clinical trial activities including patient screening, recruitment, and data collection; Ensure timely data entry and query resolution in sponsor portals; Manage regulatory document submission to sponsors and ethics committees; Coordinate study logistics including scheduling and training; Perform clinical tasks such as medication administration and diagnostic procedures; Monitor patient safety and report adverse events.
Seniority
Entry-level to Mid-level