Regional Clinical Project Manager
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Job Type | Temporary / Contract |
Location | City of London |
Area | Central London, UK |
Sector | Clinical Research |
Salary | See Job Description |
Currency | GBP |
Start Date | 01/07/2018 |
Advertiser | remoteapi |
Job Ref | BBBH675_1531472159 |
Job Views | 102 |
- Description
Regional Clinical Project Manager
Pop Science is delighted to partner again with our client in Chelsea to bring you this long-term contract to perm career opportunity As Regional Clinical Project Manager. (other levels are also available)
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 with the current projects sponsored by one of the biggest names in the pharmaceutical industry.
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 Chelsea are sought for this long-term contract to perm opportunity. (We are not looking for freelance Pm's)
As a Regional Clinical Project Manager you will ensure studies are planned and implemented to the highest standards, in compliance with ICH-GC guidelines, SOPs and all applicable regulatory guidelines.
Heres a snap shot of what you will be doing :
- To lead local/ regional study management teams guidelines, SOPs and all applicable regulatory requirements for the allocated study
- 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 and 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, TRI 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.
- Accountable for status of study/studies communicated regularly with study team and management and that unresolved issues are escalated appropriately
- Responsible for maintenance of TMF
- Preparation of site agreements, contracts, and financial/site payment tracking during study conduct.
- Protocols developed in conjunction with Chief Operating Officer and Investigators
- Attendance of and contribution to Investigator meetings
- Ensure site and outsourced CRO staff trained in protocol specific procedures
- Management of ethics, regulatory requirements and local applications
- Liaison with external customers e.g. Steering Committees, Investigators, Study Nurses and Clinical Trial Pharmacists etc.
- To provide the day-to-day operational management of CROs and vendors ensuring delivery against contracted scope of work for the allocated region
- Plan and manage study budget
- Contribute to process improvement
- Assist with training and with preparation of training material for Study support roles
The must have Skills and Experience:
- Proven clinical trials project management and leadership experience 2-3 yrs
- Life science degree
- Excellent organisational , Presentation and Supervisory skills
- Excellent interpersonal skills
- Proven ability to develop and update working practices
- Flexible and effective project management, communication and negotiation skills
- Ideally experience overseeing outsourced CRO work
- Strong understanding of cardio vascular 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.
Pop Science are an innovative, personal and experienced recruitment and staffing consultancy. Our aim is to make science more popular by championing careers in clinical and scientific research, technology, engineering, maths and more. Whether you want a permanent job, a contract role or even a change in perspective with some volunteering, contact us and let us help you. We support working practises that promote happiness at work.
We're an experienced, skilled team with personality; we have a passion for science, and drive and enthusiasm to make a difference to you.
Find out more at Pop Science - Recruitment