---
title: "Study Start‑Up Project… – Maidenhead, United Kingdom"
canonical: "https://www.metaintro.com/job/study-start-up-project-manager-client-dedicated-at-fortrea-a4df27f7-a72d-534d-ab9d-776544bfcbc8"
language: "en"
author: "Metaintro"
---

[![Fortrea logo](/api/company-logo?url=https%3A%2F%2Ffortrea.com%2Fthemes%2Fcustom%2Ffortrea%2Fimages%2Ficons%2Ftouch.png&sig=IVM-QXHNqETVc3SQgJDggKA-ttiqN0lXZSsX_2u5WCc)](/company/fortrea)[Fortrea](/company/fortrea)
# Study Start‑Up Project Manager – Client Dedicated at Fortrea

**Setup**
: Hybrid

**Location**
: Maidenhead, England

**Type**
: Full-time

**Level**
: senior

**Posted**
: Oct 2, 2026

## 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.

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