Study Startup Specialist I
Core
Coordinate clinical trial start-up activities in Taiwan, managing site contracts, regulatory documentation, and activation timelines.
Role type
Clinical research start-up specialist
Builds
Clinical studies for pharmaceutical clients
Domain
Pharmaceutical clinical trials
Deliverable
client delivery
Required skills
Clinical start-up process management, site contract negotiation, regulatory document collection, ethics committee submission support, timeline development, enrollment projection, TMF maintenance
Preferred skills
Pharmaceutical/healthcare degree background
Technologies
MS Office (Word, Excel, PowerPoint, Outlook)
Responsibilities
Maintain study tracking systems, facilitate site budgets and contract negotiations, support regulatory document collection, prepare submission dossiers for ethics committees, communicate with project teams and sites, develop startup timelines and enrollment projections, maintain Trial Master File
Seniority
Entry-level to Junior, hands-on IC
