Real World Evidence Lead (Cardio Renal Metabolic)

BoehringerPRDBracknell, EnglandOn-siteFull-timeSenior, 5–8 yearsListed 3 hours ago

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About this role

THE POSITION

As Real World Evidence Lead (Cardio Renal Metabolic - CRM), you will lead the design and implementation of a major evidence-generation programme within the CRM area. The role will support healthcare decision-making, market access and patient outcomes across the UK and Ireland, while also contributing to global scientific priorities. A key focus will be the design and delivery of a large study exploring patients’ experiences and outcomes associated with treatment. You will bring strong expertise in patient-reported outcomes, surveys and decentralised study approaches, combining scientific rigour with practical delivery across internal teams and external partners.

The position is offered on a fixed-term basis for 12 months. The role requires regular onsite presence at our Winnersh Head Office, with a minimum of 2 days per week spent working onsite.

TASKS AND RESPONSIBILITIES

- Lead the design, implementation and delivery of complex, high-quality real-world evidence and epidemiological studies that address UK, Ireland and global evidence needs.

- Identify evidence gaps and translate them into clear research questions, fit-for-purpose study designs, appropriate data sources and robust analytical approaches.

- Design and implement a large cardio-renal-metabolic study, with a strong focus on understanding patients’ experiences and outcomes associated with treatment.

- Lead the selection and use of patient-reported outcome measures, surveys and decentralised study approaches where appropriate.

- Provide scientific and operational leadership throughout the full study lifecycle, including concept development, protocol writing, internal approval, analysis, reporting and publication.

- Work closely with UK, Ireland and global colleagues across Medical, Market Access, Health Systems Engagement, Franchise and Corporate Epidemiology teams to align evidence-generation priorities.

- Manage external partners, including CROs, academic collaborators, data partners and other vendors, ensuring studies are delivered to agreed quality, timelines and budgets.

- Communicate study findings clearly to scientific, clinical, commercial, policy and executive audiences, and lead dissemination through abstracts, posters, presentations and peer-reviewed manuscripts.

- Ensure all studies comply with company policies, governance and privacy requirements, applicable regulations, BI SOPs and the ABPI and IPHA Codes of Practice.

- Manage competing priorities across a portfolio of studies while maintaining high scientific standards, effective stakeholder engagement and efficient use of resources.

REQUIREMENTS

- A degree or equivalent qualification in mathematics, statistics or a related scientific discipline, together with a relevant postgraduate qualification such as an MSc or PhD in Epidemiology or a related field.

- Extensive experience leading real-world evidence projects.

- Strong practical expertise in epidemiology, real-world evidence methods, study design, medical statistics and the analysis of large healthcare datasets.

- Proven experience delivering epidemiological studies from research proposal and protocol development through to analysis, reporting and publication.

- Pharmaceutical industry experience and experience overseeing CROs, academic collaborators, data partners or other external vendors.

- Excellent written and verbal communication skills in English, with the ability to explain complex scientific concepts clearly to varied audiences.

- Strong stakeholder management, influencing and negotiation skills, with a collaborative and proactive working style.

- The ability to prioritise effectively and work across a portfolio of complex studies.

- Direct experience in obesity and/or cardio-renal-metabolic disease research would be highly desirable.

- Knowledge of UK real-world data sources and the UK healthcare environment would be beneficial.

- Experience designing and delivering patient-reported outcome or survey-based research would be advantageous.

WHY THIS IS A GREAT PLACE TO WORK

Boehringer Ingelheim has been recognised as a Top Employer in the UK, demonstrating our commitment to building an exceptional workplace through strong people practices and supportive HR policies. To learn more about why BI is a great place to work, visit: https://www.boehringer-ingelheim.co.uk/careers/uk-careers/why-great-place-work