Real World Evidence Lead (Cardio Renal Metabolic)

Boehringer Ingelheim
Boehringer Ingelheim logo
Location
Bracknell Forest
Job Type
Full-time
Posted
October 6, 2026
Views
3

Job Description

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.

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

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Frequently Asked Questions

Where is the job located, and what is the work-mode policy?
The job is located in Bracknell Forest. It is a hybrid role requiring regular onsite presence at the Winnersh Head Office, with a minimum of 2 days per week spent working onsite.
What are the key responsibilities of this role?
You will lead the design, implementation, and delivery of complex real-world evidence and epidemiological studies. Key tasks include designing a large cardio-renal-metabolic study focused on patient experiences, managing external partners like CROs, and collaborating with internal teams to align evidence-generation priorities.
What qualifications and experience are required?
You need a degree in mathematics, statistics, or a scientific discipline, plus a postgraduate qualification (MSc/PhD) in Epidemiology or a related field. Extensive experience leading real-world evidence projects, pharmaceutical industry experience, and experience overseeing external vendors are also required.
What is the duration of this position?
The position is offered on a fixed-term basis for 12 months.

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Job Information

Source: manual
AI Relevance: 80/100 (Highly relevant)
Remote Type: onsite
Allowed Locations: Worldwide
Skills & Tags:
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