Site Activation Coordinator
Core
Execute site activation activities for investigative sites in clinical studies, ensuring regulatory document completeness and accuracy.
Role type
Site Activation Coordinator
Builds
Regulatory and contractual documents for clinical trial sites
Domain
Clinical research / Life sciences
Required skills
Regulatory document preparation, document review for accuracy, internal system database maintenance, progress tracking of ethics and ICF/IP releases, multi-project management
Preferred skills
Clinical trial environment awareness, drug development process knowledge
Technologies
MS Office applications
Responsibilities
Perform site activation tasks per SOPs and regulations, prepare and review site regulatory documents, distribute completed documents to sites and internal teams, update internal tracking tools and project plans, follow up on document approval and execution
Seniority
Entry-level, hands-on IC
