Clinical Project Manager - 3 month contract
| Job Type | Permanent Full Time |
| Location | London |
| Area | Central London, UK |
| Sector | Clinical Research |
| Salary | £40k - 60k per year |
| Currency | gbp |
| Start Date | ASAP |
| Advertiser | remoteapi |
| Job Ref | 1495 |
| Job Views | 88 |
- Description
We are urgently seeking a Clinical Project Manager who is able to work on-site in Central London. This position will be for approximately three months and is available on either a full-time or part-time basis of between 3 and 5 days per week.
Our client has an extensive global network of sites they work with to provide clinical trials to a range of sponsors and across various Therapeutic areas, although there is a focus on cardiovascular, haematology and oncology therapeutic areas.
Ideally, we are seeking a CMP III with a minimum of three years’ experience in the role — someone who can quickly adapt and provide effective support to the team in the background. Strong regulatory affairs experience (e.g., submissions) is essential.Scope of Work
- Provide short-term project management support to an ongoing clinical study, ensuring delivery within agreed timelines, budgets, and quality standards, in full compliance with ICH-GCP, SOPs, and regulatory requirements.
- Oversee study operations and vendors, including CROs, sites, and external partners, maintaining effective communication, risk management, and documentation (e.g., TMF, contracts, budgets, and reports).
- Support the Clinical Operations team with coordination, issue resolution, and preparation of key study materials, contributing to process improvement and ensuring continuity during team absences.
Essential Experience:
- 5–10 years of overall clinical project management experience within a CRO or sponsor environment.
- Proven ability to manage timelines, vendors, and multi-site studies in accordance with ICH-GCP.
- Strong communication, organizational, and problem-solving skills; experience in cardiovascular studies preferred.
- Solid experience in regulatory affairs (submissions and documentation).
- Global experience managing complex interventional and observational studies.
#clinicalresearch #clinicaltrials #pharmajobs #CROjobs #clinicalprojectmanager #clinicaldevelopment #londonjobs #clinicalstudymanagement #SCOPE2022 #decentralizedclinicaltrials #DCT #decentralizedtrials