Skip to main content
ResumeKart
← Back to Jobs

Project Coordinator Clinical Pharmacology

Fortrea•United Kingdom•🌍 Remote
Full-timeMid Level
👁️ 0 views•📝 0 applications•Posted 9/9/2026•Expires 11/8/2026
Tailor Resume for This JobCheck ATS Score

Get alerts for roles like this

More Project Coordinator Clinical Pharmacology roles in United Kingdom — straight to your inbox. No account needed.

Applying to this role? Tailor your résumé to this job description in one click, then download it free — just a small ResumeKart footer, no subscription.

Job Description

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 team generate critical safety, tolerability, PK and PD data that help new medicines to move forward Fortrea Clinical Pharmacology is hiring Clinical Project Coordinators in the UK, to drive this mission forward.

Candidates with strong organizational skills, attention to details, and the ability to manage financial processes effectively will be particularly well suited for the role. There are several roles in consideration, to work more sponsor dedicated or full service CPS and at different levels of seniority.

Job Overview

Responsible for the coordination and completion of project tasks in support of Project Management for low to medium complex studies including external site studies. Initiates creation of study specific documents (e. g. , Project Management Plan, Communication Plan, Risk Mitigation Plan).

Develops trial management tools to monitor study activity, including project setup activities, formats, posts, and compiles study timelines. Attends, schedules, and organizes study-related meetings; distributes agendas, maintains, and distributes meeting minutes, Project, and Risk Log.

Works with the document specialist team as appropriate to transfer documents in a timely manner to the Trial Master File (TMF) in accordance with applicable SOPs, policies, system, and client requirements. Assists with training and mentoring new PCs and Associate PCs.

Summary of Responsibilities: Works independently with little assistance from a more senior PC or PM in owning and developing study specific documents (e. g.

, Project Management Plan, Communication Plan, Investigator Package Plan, Risk Register, Project Specific Training Matrix, and any other applicable plans as required), including compliance with client-specific requirements, for low to medium complex studies including

Required Skills

Project ManagementRisk MitigationTrial ManagementDocument ManagementFinancial ProcessesClinical ResearchPharmacologyStudy CoordinationMeeting OrganizationTraining and Mentoring

Partner picks for Project Coordinator Clinical Pharmacology in United Kingdom

Matched to the skills this page calls for and the candidate's location.

Partner
  • Partner course provider

    University and industry courses, professional certificates and online degrees.

    covers project management
  • Partner course provider

    Certification training in cloud, data, cyber security, project management and digital marketing.

  • edXVerified partner
    Partner course provider

    Courses and programmes from universities and institutions worldwide.

Partners are ResumeKart affiliates or institutes it works with; ResumeKart may earn a commission when a candidate enrols. Placement is decided by relevance, not payment. How ResumeKart earns

The best-paying roles in your field. Every week. Free.

Get job alerts and salary insights in your inbox

We respect your privacy. Unsubscribe anytime with one click.