CPL Life Sciences are partnering with a well renowned CRO who are seeking an experienced Clinical Trial Manager to join their Trial Management team to focus on a number of studies across phases II-III. Their trial portfolio spans across a range of therapeutics areas, with expert training provided to enhance your expertise if required on specific studies.
The successful candidate will oversee the full project lifecycle, ensure compliance with industry regulations, and serve as the primary point of contact for sponsors. You will be responsible for the successful operational delivery of set goals and timescales.
Key Responsibilities:
* Oversee day-to-day trial operations in accordance with protocols and regulatory standards
* Act as the primary liaison for sponsor communication on project-specific matters
* Maintain expert-level knowledge of assigned protocols and therapeutic areas
* Provide cross-functional leadership across internal teams and departments
* Review and contribute to protocol development, data plans, and final reports
* Develop and maintain detailed project execution plans
* Proactively assess and manage project risk
* Oversee vendor activities and performance
* Ensure site quality and supervise Clinical Research Associates
* Drive timelines and deliverables while meeting project milestones
Qualifications required:
* Bachelor’s in health/life sciences (advanced degree preferred)
* Experience of direct clinical trial management
* Phases II–III experience highly desirable
* Flexible on therapy area background
* Strong leadership, organization, and communication skills
If you are open to discussing new opportunities at this time then please apply here to arrange a follow-up call to find out more.
This role is based on-site in central London, with one day working from home flexibility.