Study Startup Specialist II
Core
Coordinate clinical study startup activities in Taiwan, managing site contracts, regulatory documentation, and activation timelines.
Role type
Clinical study startup specialist
Builds
Clinical trials
Domain
Pharmaceutical clinical research
Deliverable
client delivery
Required skills
Site contract negotiation, regulatory document collection, timeline development, TMF maintenance, stakeholder communication, translation review
Preferred skills
Leadership, mentoring, relationship building
Technologies
Trial Master File (TMF)
Responsibilities
Maintain study tracking systems, facilitate site budgets, support regulatory submissions, develop startup timelines, supervise TMF maintenance
Seniority
Mid-level, hands-on IC
