Clinical Research Associate II
Core
Establish, maintain, and support clinical trials by verifying subject rights, data accuracy, and protocol compliance through site monitoring.
Role type
Clinical Research Associate II (CRA II)
Builds
Clinical study execution and data integrity for medical device and therapeutic studies
Domain
Clinical Research / Medical Device / Therapeutics
Deliverable
physical/clinical work
Required skills
Site monitoring, protocol compliance verification, multi-study management, travel logistics, regulatory knowledge (ICH-GCP, ISO14155), site relationship management
Preferred skills
Prior CRA II experience, German language proficiency, adaptability in fast-moving environments
Technologies
None stated
Responsibilities
Conduct site monitoring visits, manage site relationships across multiple protocols, support feasibility/setup/closeout activities, travel regularly to assigned sites
Seniority
Mid-level IC