Medpace is a leading clinical contract research organization (CRO) and is expanding its Clinical Trial Management Group in the United Kingdom. The role is available in London and Stirling with remote flexibility for qualified candidates. Competitive salary/bonus, equity grants and a supportive career path are offered.
Responsibilities
* Manage and provide accountability for day‑to‑day operations of the project, as defined by the contract and according to ICH/GCP and all applicable regulations.
* Serve as primary Sponsor contact for operational project‑specific issues and study deliverables.
* Maintain in‑depth knowledge of protocol, therapeutic area, and indication.
* Provide cross‑functional oversight of internal project team members and deliverables, including ensuring all necessary project‑specific training is provided.
* Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable.
* Develop operational project plans.
* Manage risk assessment and execution.
* Responsible for management of study vendor.
* Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables.
Qualifications
* Bachelor’s degree in a health or life science‑related field; advanced degree preferred.
* Experience in Phases 1‑4, with a preference for Phases 2‑3.
* Minimum of 2 years of Clinical Trial Management experience; CRO experience preferred.
* 5 + years of Project Manager/Clinical Trial Manager experience at a CRO required for a remote‑based role.
* Management of overall project timeline.
* Bid defense experience preferred.
* Strong leadership skills.
Benefits
* Competitive salary/bonus program and equity grants.
* Remote flexibility (after probation) and flexible work environment.
* Competitive PTO packages.
* Structured career paths with opportunities for professional growth.
* Company‑sponsored employee appreciation events.
* Employee health and wellness initiatives.
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