Studienkoordinator klinische Forschung (m/w/d)
Core
Planning, organizing, and coordinating resources for clinical trials, including feasibility assessments and quality control of study documents.
Role type
Clinical research study coordinator
Builds
Clinical trial operations and data management
Domain
Healthcare / Clinical Research
Required skills
Resource planning, feasibility assessment, quality control, medical support, staff coordination, document management
Preferred skills
Intensive care or anesthesia specialization, complex study workflow experience, SOP knowledge
Technologies
Clinical trial management systems, SOPs
Responsibilities
Plan and organize resources for clinical trials, create study schedules and data documents, conduct feasibility checks for facilities and staff, provide medical support to participants, guide and coordinate study staff, perform quality controls on study documents
Seniority
Mid-level, hands-on IC