Senior Clinical Research Associate
Core
Conducting onsite monitoring visits, driving study startup, and ensuring subject safety, rights, and data compliance for Phase II/III clinical trials.
Role type
Senior Clinical Research Associate (IC)
Builds
Clinical trial data and regulatory documentation
Domain
Clinical Research / Life Sciences
Required skills
Onsite monitoring, Source document verification, CRF review, Query resolution, Site management, Feasibility research, Regulatory document preparation, Phase II/III trial experience, Czech language fluency, English language fluency, Driver's license
Preferred skills
Oncology study experience, Multitasking, Team collaboration
Technologies
MS Office
Responsibilities
Conducting and reporting onsite monitoring visits, Driving study startup phase, Performing CRF reviews and source document verification, Managing site communication and schedules, Supporting quality control and compliance monitoring, Participating in feasibility research, Supporting regulatory submissions
Seniority
Senior, hands-on IC