Description
The Study Start‑Up PM will lead country-level regulatory submissions, approvals, IRB/IEC and regulatory authority interactions, local documentation, compliance, timelines, site readiness, clinical and ancillary supplies, and country data for a global, client-dedicated clinical research program. The role requires at least five years of clinical research experience with strong study start-up and regulatory exposure, knowledge of local regulatory environments, independent project management, stakeholder management, and a bachelor’s degree in a relevant field. It is based in London with a hybrid arrangement requiring 2–3 days onsite per week.
