RWE / Epidemiology Lead

Description

Your new company

You'll be joining a global biopharmaceutical organisation dedicated to improving outcomes for patients through evidence–driven healthcare decisions. You'll work within a highly collaborative environment, contributing to real–world evidence generation that supports clinical development, regulatory strategy, market access, and scientific understanding of multiple diseases, including rare disease.

Your new role As a Real World Evidence / Epidemiology Lead, you will lead and support the design, delivery, and communication of real–world evidence studies across a diverse portfolio of projects, primarily focused around the company's rare disease projects.

This position offers significant autonomy and would suit candidates ranging from experienced epidemiologists through to established RWE leaders looking for a hands–on scientific role.This is initially a 6 month contract that may extend and can be done on a remote basis within the UK (candidates CANNOT be based outside of the UK).

Key responsibilities include:

Designing and delivering global RWE studies across areas such as epidemiology, disease burden, natural history, care pathways, unmet need, and real–world effectivenessLeading studies from concept development through to reporting, publication, and stakeholder communicationDeveloping study concepts, protocols, statistical analysis plans, and governance documentationCollaborating with academic partners, medical experts, vendors, statisticians, and internal stakeholdersSupporting the growth and development of disease–specific real–world data assets and registriesProviding scientific leadership on methodology selection, study design, and data source evaluationInterpreting study results and communicating findings to both internal and external audiencesEnsuring studies are delivered on time, to budget, and in line with quality and governance requirements

What you'll need to succeed

A successful candidate will bring strong experience in real–world evidence generation together with the ability to operate independently across complex projects.

Proven experience delivering RWE studies using primary and/or secondary data sourcesExperience gained within pharmaceutical companies, specialist consultancies, CROs, academic research groups, or recognised centres of excellenceStrong understanding of epidemiology, observational research methods, and outcomes researchExperience developing study protocols, analysis plans, and scientific publicationsAbility to work effectively with academic collaborators, KOLs, and multidisciplinary teamsStrong project management and stakeholder management capabilitiesExcellent scientific communication skillsThe right to work in the UK without restriction until at least February 2027 (no sponsorship is available for this role)

The following would be advantageous:

PhD (or equivalent experience) in Epidemiology, Public Health, Outcomes Research, Health Economics, or a related disciplineExperience working with rare diseasesExperience with patient–reported or caregiver–reported dataExperience supporting disease registries or longitudinal observational studiesExperience collaborating with academic institutions and international research networks

What you'll get in return

As well as the chance to make a strong impact on the company's portfolio, you'll be supported by a highly experienced team and have very flexible working arrangements.

What you need to do now

If you're interested in this role, click 'apply now' to forward an up–to–date copy of your CV, or call us now.

If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.

Ad ID: 5418762800