Evidence Generation Study Manager - RWE

An opportunity to play a key role in the design and delivery of primary real-world evidence (RWE) studies for a global healthcare organisation with a mission to give patients greater control over their health through knowledge, choice, and connection.

The Role
This position will lead the end to end operational management of primary RWE studies with a strong focus on patient enrolment projects such as non interventional studies, registries, and hybrid or decentralised designs. You’ll oversee all aspects of delivery from start to end, ensuring timelines, budgets, and compliance standards are met. Working cross functionally across Clinical, Data, Quality, and Commercial teams, you’ll ensure studies generate robust, real world insights that ultimately improve patient outcomes.

Key Responsibilities

• Serve as the primary operational lead for patient enrolment studies and client facing project delivery
• Build and execute operational plans for prospective RWE projects, ensuring regulatory and ethical compliance
• Lead study start-up, including protocol implementation, site identification and activation, EDC build, and vendor oversight
• Ensure effective patient recruitment, data collection, and risk management across all sites
• Drive cross-functional collaboration to ensure cohesive study execution and high data quality
• Support business development activities by contributing to bid preparation and client meetings
• Champion process improvement and support the strategic evolution of the Evidence Generation function

Experience & Profile
You’ll bring significant experience in delivering primary, patient enrolment real world studies, ideally across a range of non interventional and observational designs. A strong understanding of clinical operations, site management, and vendor coordination is essential, alongside a solid grasp of regulatory frameworks (ICH-GCP, GDPR, ethics submissions).

Experience in registry set up, hybrid or virtual trial delivery, and patient engagement strategies will be highly valued. You’ll be confident leading complex, multi stakeholder projects and comfortable working within a fast paced, collaborative environment.

Formal project management training (e.g. PRINCE2, PMP) and proficiency with CTMS, eTMF, and EDC systems are desirable. A degree in life sciences is required; an advanced or clinical qualification is preferred.

What’s on offer?

• Opportunity to shape and deliver global RWE studies that directly engage patients

• Exposure to innovative study designs and decentralised research approaches

• Collaborative, mission driven culture focused on patient outcomes

• Competitive compensation and hybrid working flexibility

Could this be the role for you?

If you’re ready to lead impactful, patient enrolment RWE studies that generate meaningful real world insights, we’d love to hear from you. Hit apply to submit your CV, or reach out directly for a confidential discussion.

Unless otherwise stated, if applying for a job within the UK or European Union, you must ensure that you are already authorised to work there.
Carrot Recruitment acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, colour, sex, age, national origin, religion, sexual orientation, gender identity and/or expression.

If there are any arrangements or adjustments we can make to assist you at interview then please let us know and we’ll be more than happy to assist.