Clinical Trial Coordinator
Core
Administrative and technical support for clinical trial project activities, acting as a cross-functional liaison and study lead.
Role type
Clinical Trial Coordinator
Builds
Clinical trial documentation, regulatory submissions, and study metrics reports
Domain
Clinical Research / Pharmaceutical Trials
Deliverable
client delivery
Required skills
Regulatory document review, (e)TMF management, study metrics analysis, vendor tracker maintenance, ISF/Pharmacy binder coordination, translation QC, meeting organization
Preferred skills
Study lead experience, process improvement initiatives, cross-functional liaison duties
Technologies
GoBalto, eTMF, MS Office (Word, Excel, PowerPoint), clinical trial database systems
Responsibilities
Coordinate assigned trial activities per task matrix, perform file reviews (department/Internal/Country/Investigator), ensure tasks are completed on time and within budget, communicate project risks, maintain study documentation and system access, support RBM activities, process documents for client (e)TMF, track local regulatory documents, transmit documents to IRB/IEC, analyze and reconcile study metrics, assist with site documentation resolution, coordinate study supplies to sites
Seniority
Mid-level, hands-on IC