Clinical Trial Project Manager
Core
Manage day-to-day operations of clinical trials for biotech and pharmaceutical companies, ensuring compliance with ICH/GCP regulations and delivering study outcomes.
Role type
Senior IC clinical trial project manager
Builds
Clinical trial deliverables for biotechnology, pharmaceutical, and medical device industries
Domain
Clinical research / Biopharma
Required skills
Clinical trial management, protocol knowledge, risk assessment, vendor management, site quality oversight, cross-functional team leadership, regulatory compliance (ICH/GCP), project planning
Preferred skills
Bid defense experience, management of Phases 2-3 trials, advanced degree in health-related field
Technologies
Clinical trial management systems, regulatory compliance frameworks
Responsibilities
Manage and provide accountability for day-to-day operations of the project, Serve as primary Sponsor contact for operational project-specific issues, Review and provide input for study protocol and final study report, Develop operational project plans, Manage risk assessment and execution, Manage site quality including supervision of Clinical Research Associates
Seniority
Mid-level, hands-on IC