What if your project leadership skills helped new medicines take their first step in human clinical trials?Fortrea is one of the world´s largest and longest-established early-phase clinical research organizations.From first-in-human to exploratory biomarker or complex ph1b programs, our Clinical Pharmacology teams generate critical safety, tolerability, PK and PD data that help new medicines to move forward.We are currently hiring a Project Manager I and a Project Manager II in the UK to drive this mission forward.This is a full-time, remote job.DAILY RESPONSIBILITIESLead the end-to-end delivery of assigned Healthy Volunteers and Patient Clinical Pharmacology projects independently or under the direction of a Senior Project Lead, overseeing complex, high‑value studies across regional / global, cross‑functional teams.Act as the primary point of contact for sponsor project teams, managing expectations, driving communication, and building long‑term client relationships.Own project scope, timelines, and budgets , proactively managing change, financial performance, and delivery against contractual commitments.Apply your project leadership expertise to anticipate, identify, and mitigate risks , managing critical paths to ensure key milestones and performance metrics remain aligned with both client and Fortrea objectives.Provide senior leadership within a matrix project environment , guiding and mentoring project team members while resolving issues and escalations at pace.Ensure quality, compliance, and audit readiness , maintaining oversight of TMFs, CTMS activities, project training, and adherence to SOPs and ICH/GCP standards.Contribute to business growth and operational excellence , supporting bid defence activities, strategic client relationships, KPI oversight, and process improvement initiatives.AND YOUR LONG-TERM CONTRIBUTION?You will play a key role in strengthening how Fortrea delivers Phase Ib clinical trials , helping evolve our approach to more complex early‑phase programs.Beyond individual projects, your experience will support process innovation and operational delivery , influencing how Phase Ib studies are planned, executed, and scaled across Clinical Pharmacology Services.WHO YOU AREFor Project Manager II , we need you to bring extensive clinical research experience within a CRO or biopharmaceutical environment, including at least 2 years of full project management accountability on domestic, regional and or international clinical studies.For Project Manager I, at least 4 years of clinical research experience in a pharmaceutical company/CRO, including a minimum 1-2 years of experience working in a project management environment.Phase 1 and Phase Ib experience : Familiarity with early-phase trials in healthy volunteers and patients and their fast-paced environment is ideal, but international PM experience in Ph II-III will also be welcomed.Financial Acumen : study budget management skills, with experience in forecasting, revenue recognition and change order development and negotiation.Leadership : proven ability to inspire and manage globally dispersed teams and vendors, ensuring cross-functional collaboration and achieving core project milestones. Ability to work on multiple studies at any one time.Risk Management : expertise in critical path analysis and the development of effective risk mitigation plansClient Relations : a probing ability to build client trust, resolve complex challenges and influence decisionsBID presentation expertise.Education/Qualifications:University/college life science degree from an appropriately accredited institution.Preferred :Master´s or other advanced degreePMP certificationLearn more about our EEO & Accommodations request here .
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