Clinical Project Manager / Senior Clinical Project Manager

  • Location


  • Sector:

    Life Sciences

  • Salary:


  • Contact:

    Chris Brough

  • Contact email:

  • Job ref:


  • Published:

    over 1 year ago

  • Expiry date:


  • Startdate:

    May 2021

  • Liquid error: internal
Volt International are looking for an experienced Clinical Project Manager or Senior Clinical project Manager to join our growing client, working remotely from the UK and FULLY HOME BASED

The Clinical Project Manager would be responsible for the overall coordination and management of a range of clinical trials from start up through to close. This position directs the technical and operational aspects of clinical projects.


Lead the project team, ensuring the project is delivered according to the clients timescale.
Create and execute project management plans required for project delivery and in accordance with processes
Ensure quality and adherence to the relevant policies, SOPs, and working instructions, GCP and regulatory guidelines.
Establish clear lines of communication and escalation pathways, and effectively communicate with project stakeholders
Provide input on study related documents such as the study protocol, CRF, Medical Review/Monitoring plan, and Clinical Study Report
Lead internal and external meetings with internal and sponsor teams
Manage vendors and vendor relationships
Ensure effective and efficient resource utilisation across projects and programs
Produce, maintain and circulate project progress and status reports
Manage the study budget

Serve as the primary point of communication between the sponsor and project team

Lead by example and encourage team members to develop strong solutions for clinical trial delivery

Responsible for oversight of project team delivery and communication with functional managers, including performance feedback


Minimum Bachelor's degree in life science, healthcare and/or business degree
Minimum 5 years of experience in clinical research or drug development, with at least 2 years of clinical trial project management experience
CRA experience preferable
Expert knowledge of ICH-GCP(R2), data and patient privacy practices, and applicable (local) regulatory requirements


Excellent written and verbal communication, planning, critical thinking and organisational skills, including command of English language
Demonstration of good financial acumen, administrative excellence and strong analytical skills
Representative, outgoing and client focused
Ability to work effectively in a fast-paced challenging environment within a growing company
Computer literate (MS Word, Excel and PowerPoint essential)
Strong presentation skills
Committed to helping other develop alongside your own progression
Dependable and able to take action to quickly to address urgent needs
Proactive and solution oriented
Willingly takes ownership and drive positive, collaborative results within the project team

Must have the Right to Work in the UK