Global Clinical Project Managers

Pop Science is delighted to partner with our client in London to bring you this long-term contract to perm career opportunity As Global Clinical Project Manager

Candidates must be experts in clinical research and have the right to work in the UK to be considered for this role.

This organisation focuses on Haematology and Cardiovascular projects and currently have new studies in the start-up phase and large studies in closing phases too. The role provides a great opportunity to manage and develop a study team and work within global cardiovascular observational studies.

Truly exceptional candidates who are happy to be office based in West London are sought for this long-term contract to perm opportunity.

Global (Clinical) Project Manager will lead global study management teams, ensure studies are planned and implemented to the highest standards, in compliance with ICH-GC guidelines, SOPs and all applicable regulatory guidelines.

Here is a snapshot of what you will be doing:

• Define and monitor project scope, timelines and deliverables from project initiation to close out. Ensure project plan aligns with contract requirements, and address any reconciliation required
• Study oversight and status reporting study targets discussed as agreed includes the development of study timelines, communication, risk and quality plans, team training and oversight
• Schedule, plan for and document regularly scheduled project team meetings. Assess project issues, propose resolutions to the project team, management and Steering Committee as necessary, and then track implementation of resolution through to completion.
• Ensure the overall quality of project services and deliverables by documenting project/clinical trial progress to ensure completeness of documentation and data collection, management of supplies and resources in adherence with the project timelines, budgets and quality standards including central laboratory (if applicable) and contract/academic research organisations
• Responsible for maintenance of TMF
• Accountable for the status of study/studies communicate regularly with study team and management and that unresolved issues are escalated appropriately
• preparation of site agreements, contracts, and financial/site payment tracking during study conduct
• Protocols developed in conjunction with Chief Operating Officer and Investigators

You should recognise yourself here:

• Proven clinical trials project management and leadership experience
• Life science degree - Excellent organisational and presentation skills -Line management and Supervisory experience -Practical coaching/training experience
• 4 years in Regional Clinical Project Management role
• Proven ability to develop and update working practices
• Flexible and effective project management, communication and negotiation skills
• Strong experience overseeing outsourced CRO work
• Understanding of cardiovascular disease and treatment
• Candidates must be experts in clinical research and have the right to work in the UK to be considered for this role.

Contact Bryan on 01273 729819 apply with CV current and expect salary bryan@pop-science.co.uk or Gail on info@pop-science.co.uk 07971666239

Please ask for full vacancy details

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