Clinical Trial Coordinator Intern
Core
Administrative and technical support for clinical trial site activation, audit readiness, and study documentation management.
Role type
Clinical Trial Coordinator Intern
Builds
Study documentation, site activation plans, and regulatory compliance files for pharmaceutical and biotech clients.
Domain
Clinical Research / Life Sciences
Required skills
Site activation coordination, (e)TMF management, regulatory document review, study metrics analysis, vendor tracker maintenance, meeting organization
Preferred skills
Life Sciences degree, local language proficiency, translation support
Technologies
CTMS, Activate, eTMF
Responsibilities
Coordinate assigned trial activities per task matrix; perform department and Investigator file reviews; ensure tasks are completed on time and within budget; maintain study-specific documentation and global support systems; support RBM activities; process documents for client (e)TMF; transmit documents to client and IRB/IEC; analyze and reconcile study metrics; assist with ISF and Pharmacy binder distribution.
Seniority
Intern, 0-1 year experience