Senior Clinical Research Associate II/III (m/w/d), Multi-Sponsor, Germany
Core
Conduct monitoring on complex clinical trials for various pharma companies to assure adherence to GCP and study protocols.
Role type
Senior Clinical Research Associate (monitoring)
Builds
Clinical trial data integrity and regulatory compliance for diverse sponsors
Domain
Life sciences / Clinical research
Required skills
Site selection and initiation, Monitoring visits, Subject recruitment planning, Regulatory compliance (GCP/ICH), Data query resolution, Therapeutic knowledge
Preferred skills
Strategic site relationship management
Technologies
CRF systems, Regulatory submission tools
Responsibilities
Perform site selection, initiation, monitoring and close-out visits; Support subject recruitment plan development; Evaluate site practices against GCP/ICH guidelines; Track regulatory submissions, recruitment, and data completion; Collaborate with study sites and client representatives
Seniority
Senior, hands-on IC
