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Senior Clinical Project Manager Line Management - North London Area

Posted 25 April by Barrington James Limited Easy Apply Ended

Job Title: Senior Clinical Project Manager

Location: Home Based / UK

Salary: On Application

Company: CRO/Consultancy

I’m currently partnering a growing, global CRO with a high commitment to quality and successful delivery of clinical trials. They have a great ethos and dedication to building solid, long term partnerships with their clients operating with transparency and flexibility whilst always making sure the patient is kept at the forefront.

With global reach and broad selection of service offerings they have a good foothold in the clinical industry, but are looking to expand and a key element is to hire strong talent within Clinical Operations/Project Management.

Core Functions (but not limited to):

  • Manage all operational aspects for implementation of clinical trial activities from study start-up through database lock
  • Lead global and/or regional Clinical Study Management Team(s) in implementation of clinical trials
  • Liaise cross functionally with the Medical, Regulatory Affairs & Drug Safety, Medical Affairs and Clinical Operations staff
  • Client first point of contact and maintain regular contact with clients by means of regular visits or TCs
  • Keep and maintain records on the projects, coordinate meetings and TCs, circulate contact reports, raise purchase orders, track invoices and overall project progress
  • Manage study-related vendors
  • Provide input into and/or develop study related materials
  • Site budget negotiations and contracts
  • Perform and/or overseeing site monitoring visits for clinical trials when needed
  • Review monitoring reports, protocol deviations and data listings for allocated studies to ensure reliable quality data are delivered; coordinating with Sponsor on site selection, IRB submissions, site initiation and close-out planning
  • Track patient recruitment and progress to study timelines; supporting safety reporting and ethics committee submissions; maintain and report metrics for clinical site performance
  • Provide oversight to staff maintaining clinical trial master files to ensure their compliance with required regulatory and GCP quality standards and consistency with CRO SOPs
  • Be involved in business development activities, attend BIDs, working closely with Business Development Team to help secure new clients and projects


  • At least 4 years of Clinical Project Management in a CRO (full service) plus a CRA/Monitoring background
  • Life science degree
  • Oncology experience is a bonus but not essential
  • Strong GCP knowledge
  • Vendor management including internal contractors
  • Ability to solve issues proactively in a fast paced environment, both independent and in a team
  • Line management experience would be a bonus, plus ability to coach CRAs and Project Managers
  • Advanced knowledge of drug development process and clinical study phases and competent level of clinical research literacy and use of terminology

To apply, please email

Reference: 34997612

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