Description
The Study Startup Specialist will lead country-level study activation by supporting clinical research teams, managing site documents and TMF submissions, assisting with feasibility and site identification, coordinating agreements and budgets, preparing IP-RED packages, overseeing initial investigational product distribution, and meeting site activation targets. The role requires a Life Sciences degree or equivalent education and experience, at least two years of full-scope study startup experience in the country or region, English proficiency, and strong communication, organizational, negotiation, and relationship-building skills.
