Fortrea, one of the world’s largest and longest‑established early‑phase clinical research organizations, is hiring a Project Manager I or II in Leeds, United Kingdom, to lead end‑to‑end delivery of Healthy Volunteers and Patient Clinical Pharmacology studies. This full‑time remote role involves acting as the primary point of contact for sponsor project teams, owning project scope, timelines and budgets, and proactively managing risks in a global, cross‑functional environment. You will ensure quality, compliance, and audit readiness across TMFs, CTMS activities, project training, and adherence to SOPs and ICH/GCP standards, while contributing to bid defense and process improvement initiatives. For Project Manager II, we seek extensive clinical research experience within a CRO or biopharma, including at least 2 years of full project management accountability on domestic, regional or international studies. For Project Manager I, at least 4 years of clinical research experience in a pharmaceutical company or CRO, including 1–2 years in a project management setting. Phase 1 and Phase Ib experience is ideal; international PM experience in Phase II–III is welcome. Strong financial acumen (budgeting, forecasting, revenue recognition and change orders), leadership of globally dispersed teams, and a proven ability to manage multiple studies are essential. A life‑science degree is required, with a Master’s degree and PMP certification preferred.

Fortrea, one of the world’s largest and longest‑established early‑phase clinical research organizations, is hiring a Project Manager I or II in Leeds, United Kingdom, to lead end‑to‑end delivery of Healthy Volunteers and Patient Clinical Pharmacology studies. This full‑time remote role involves acting as the primary point of contact for sponsor project teams, owning project scope, timelines and budgets, and proactively managing risks in a global, cross‑functional environment. You will ensure quality, compliance, and audit readiness across TMFs, CTMS activities, project training, and adherence to SOPs and ICH/GCP standards, while contributing to bid defense and process improvement initiatives. For Project Manager II, we seek extensive clinical research experience within a CRO or biopharma, including at least 2 years of full project management accountability on domestic, regional or international studies. For Project Manager I, at least 4 years of clinical research experience in a pharmaceutical company or CRO, including 1–2 years in a project management setting. Phase 1 and Phase Ib experience is ideal; international PM experience in Phase II–III is welcome. Strong financial acumen (budgeting, forecasting, revenue recognition and change orders), leadership of globally dispersed teams, and a proven ability to manage multiple studies are essential. A life‑science degree is required, with a Master’s degree and PMP certification preferred.