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Project Manager II

Fortrea
Remote, GBR
Full-time
Mid · 2+ years experience
Remote
Discovered 2 weeks ago
CTMSTMFSOPs
Free

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DAILY RESPONSIBILITIES

  • Lead 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 ARE

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.

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 plans

Client Relations : a probing ability to build client trust, resolve complex challenges and influence decisions

BID presentation expertise.

Education/Qualifications:

  • University/college life science degree from an appropriately accredited institution.

Preferred

Master´s or other advanced degree

PMP certification

#LI-CV1

#LI-Remote

Learn more about our EEO & Accommodations request here .

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