Studienkoordinator (m/w/d)
Core
Coordinating and managing clinical trials in a healthcare setting, ensuring compliance with GCP guidelines and study protocols.
Role type
Study Coordinator (Clinical Trials)
Builds
Clinical trial operations and patient data management
Domain
Healthcare / Clinical Research
Required skills
GCP compliance, study protocol management, patient coordination, data entry and management, audit preparation, medical-technical examination organization
Preferred skills
Study Nurse certification, MS Office, English language skills, electronic health record system proficiency
Technologies
MS Office, electronic protected administration systems
Responsibilities
Conduct and support clinical trials per GCP guidelines, prepare and accompany study initiations, collaborate with review board members, serve as contact for sponsors/monitors/patients, manage medical file and study folders, schedule visits and coordinate examinations, independently collect and prepare data per GDPR, prepare for audits and inspections, instruct and advise study patients, organize and conduct medical-technical examinations