Clinical Project Coordinator
Core
Full-time Clinical Research Project Coordinator supporting day-to-day clinical trial management, site activation, and data maintenance for biotech and pharmaceutical clients.
Role type
Clinical Project Coordinator (IC)
Builds
Clinical trial operations and documentation for biotechnology, pharmaceutical, and medical device clients
Domain
Clinical Research / CRO / Life Sciences
Required skills
Clinical trial management, CTMS updates, eTMF management, site feasibility assessment, study supply management, status reporting, cross-functional communication
Preferred skills
Prior experience as a Study Coordinator, pharmaceutical industry background
Technologies
CTMS, eTMF, Microsoft Excel, Microsoft Word, Windows
Responsibilities
Engage in clinical trial management on a day to day level; Work closely with the project CTM for timely delivery of recurrent tasks; Compile and maintain project-specific status reports; Update CTMS with study milestones and enrollment projections; Update eTMF and perform ongoing eTMF QC; Support Clinical Trial Manager to draft study plans and guidance documents; Manage site feasibility, site activation preparation and study supply management; Communicate with regional cross functional team, vendors and sponsor effectively.