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Carrot Recruitment in the United Kingdom is seeking an experienced Manager – Operations & Data within its Real-World Evidence team. The role focuses on overseeing EDC systems, data integrity and compliance across observational studies for pharmaceutical clients.
Based in Manchester or London with hybrid work (2–3 days in the office), the post offers £45,000 plus benefits and scope to move beyond hands-on data handling into systems oversight and process improvement.
Manager – Operations & Data | Real-World Evidence
Manchester or London – £45,000 + Benefits
Are you experienced in clinical research data management, with a strong understanding of Electronic Data Capture (EDC) systems, data integrity and compliance?
We're supporting a well-established global healthcare research consultancy looking to appoint an Operations Manager (Data) within its Real-World Evidence team. This could suit an experienced Clinical Data Specialist, Data Manager or EDC Systems professional looking to take on broader responsibility for data management processes and systems oversight.
The role will focus on overseeing EDC systems, supporting research teams with data management processes and ensuring best practice around data integrity, compliance and quality across observational research studies.
Role Summary
You'll work across a team delivering bespoke observational research studies for pharmaceutical clients, providing specialist support and guidance on EDC systems, data management and operational processes.
The position sits independently of the project management teams, allowing you to provide oversight of data management practices, support internal reviews and advise colleagues on appropriate systems and processes.
The role is less focused on hands‑on data analysis or statistical programming and more around ensuring research data is collected, managed and maintained appropriately.
Your responsibilities will include:
Requirements
The key requirement is strong experience in clinical or pharmaceutical research data management, particularly involving EDC systems and an understanding of data integrity and compliance.
Experience in Real-World Evidence (RWE), observational research studies or EDC system design/configuration would be particularly advantageous.
The team is also open to considering candidates from clinical trials or CRO environments, provided they have strong transferable data management and EDC systems experience.
What's in it for you?
This could be an interesting opportunity for someone looking to move beyond day‑to‑day clinical data management into a position with greater responsibility for EDC systems oversight, data integrity and operational best practice.
You'll work across a variety of observational research studies, supporting different project teams and acting as a key point of contact for data management and systems-related matters.
The independent nature of the role also provides an opportunity to contribute to process improvement, quality standards and the wider development of data management practices within an established healthcare research consultancy.
Location & Package
The role can be based in either Cheshire (preferred), or London.
This is a hybrid working opportunity - 2-3 days a week in the office.
£45,000, alongside a wider benefits package.