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Fortrea

Global CRO providing Phase I-IV trials

Senior Clinical Research Physician

Physicians & SurgeonsConfirmed live in the last 24 hours
Full-timeLeeds, UK

About the Job

Requirements

  • Established experience as a Principal Investigator in Phase I clinical trials within an early-phase unit, including hands-on PI experience in healthy-volunteer studies.
  • Full General Medical Council registration and a current licence to practise medicine in the UK.

Responsibilities

  • Take responsibility for assigned studies from start-up through closeout and the Clinical Study Report, working as Principal Investigator or Project Physician.
  • Join sponsor start-up meetings, review protocols and Investigator Brochures, assess feasibility, and support ethics and Medicines and Healthcare products Regulatory Agency submissions.
  • Work collaboratively with the wider Fortrea team, including members from Medical Science, Project Management, Regulatory, Clinical Operations, Clinical Research Nurses and Pharmacy.
  • Screen participants, assess their eligibility, and provide medical oversight throughout their involvement in the study.
  • Ensure studies are conducted according to protocol, International Council for Harmonisation Good Clinical Practice, and internal standard operating procedures across all clinical activities.
  • Work closely with nursing and pharmacy to support the five Rs of dosing and correct delivery of the investigational product.
  • Review adverse events, assess severity and causality, prepare serious adverse-event reports when required, and contribute to safety decisions.
  • Provide study updates to sponsors and clinical research associates, support decision-making, and collaborate to identify and resolve issues during study conduct.
  • Maintain accurate source documentation, resolve data queries, and address issues as studies progress.
  • Work with the clinical research associate and study team to ensure outstanding issues and data queries are resolved during study closeout.
  • Contribute to the Clinical Study Report and confirm that the study was conducted according to protocol and accurately reported.
  • Share expertise with the Physician Associate and less experienced physicians.
  • Represent the organization at scientific conferences, advisory boards and industry consortia.

Desired Qualifications

  • A Diploma in Human Pharmacology or Pharmaceutical Medicine.
  • A Certificate of Completion of Training, or equivalent, in Clinical Pharmacology or Pharmaceutical Medicine.

About the Company

Fortrea

Global CRO providing Phase I-IV trials

Fortrea is a global contract research organization that provides clinical development services for the life sciences industry. It offers full service, functional service, and hybrid outsourcing models across Phase I–IV trials, clinical pharmacology, and consulting, serving biotech, biopharma, medical devices, and diagnostics. Its work is delivered through a network of investigators and specialized teams in approximately 100 countries, supporting trial design, execution, data management, and regulatory compliance. Fortrea’s approach combines its legacy experience from Covance and Labcorp with a pureplay CRO model to deliver fit-for-purpose solutions and agile project delivery. This positions it to manage trials across more than 20 therapeutic areas with scientific rigor and operational excellence. The company aims to bring predictability to clinical trial execution and help clients turn research ideas into real-world outcomes.

Company size
10,001+
Company stage
IPO
Headquarters
Winston-Salem, NC
Founded
2023

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