Clinical Trials Coordinator
Core
Support trial and site administration across the clinical trial lifecycle, including document management, supply coordination, regulatory submissions, and budgeting.
Role type
Clinical Trials Coordinator
Builds
Clinical trial operations and site readiness
Domain
Healthcare / Clinical Research
Required skills
Clinical Trial Management, ICH-GCP Guidelines, Regulatory Compliance, Document Management, Budgeting, Contract Negotiation, Clinical Trial Documentation, Clinical Data Management, Clinical IT, Data Analysis
Preferred skills
None stated
Technologies
MS Office, Excel, Clinical Trial Management Systems, eTMF, Training Portals
Responsibilities
Track essential documents and report safety reports; Collate, distribute, and archive clinical documents including eTMF; Prepare submission packages for Ethics and Regulatory Agencies; Develop and control country and site budgets; Negotiate and maintain contracts with investigators; Organize local investigator meetings; Update Clinical Trial Management Systems.
Seniority
Individual Contributor
