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Real world evidence generation study manager

Newcastle Upon Tyne (Tyne and Wear)
Carrot Recruitment
Study manager
Posted: 30 August
Offer description

Evidence Generation Study Manager

Location: Remote, UK



**Note - experience of working within RWE is essential for this role - please only apply if you have genuine experience in this area**



An opportunity for a commercially aware, delivery-focused project manager to lead global real-world evidence (RWE) studies within a collaborative and fast-moving environment. This role combines strategic thinking, operational oversight, and direct client engagement — ideal for someone who thrives on delivering complex studies to a high standard.


The Role

You’ll take ownership of RWE study delivery from end to end, overseeing design, start-up, vendor management, data quality, and close-out across a range of study types (non-interventional studies, registries, decentralised/virtual studies, and occasionally interventional trials). You’ll also support pre-award work, including bid writing and client meetings, and contribute to the development of the broader Evidence Generation function.


Key Responsibilities:

* Lead day-to-day operational delivery across multiple global RWE projects
* Build and manage project plans, timelines, budgets and resourcing
* Act as primary contact for clients and internal teams on all operational matters
* Oversee vendors (including EDC build, site set-up, regulatory, data, etc.)
* Ensure full compliance with ICH-GCP and internal SOPs
* Support bid development and client pitches as an operational SME
* Contribute to shaping departmental processes and strategy


Skills & Experience Required:

* Bachelor’s degree in Life Sciences or related field (clinical or advanced degree preferred - (RN, MPH, MS, MA, MBA, PharmD)
* In-depth experience delivering real-world evidence or late-phase studies
* Formal project management qualification (e.g., PRINCE2, PMP)
* Solid knowledge of ICH-GCP and regulatory expectations for non-interventional research
* Strong grasp of clinical operations platforms and systems (CTMS, eTMF, EDC, QMS)
* Experience in matrixed environments and cross-functional project teams
* Strategic thinker with hands-on delivery skills — comfortable balancing both
* Clear communicator with a collaborative, solutions-oriented approach


If you’re looking for a role that mixes study delivery with strategic input and client visibility and you’ve got the clinical and operational credibility to back it up, this could be a strong match. I look forward to hearing from you.

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