Posted 21 July, 2026
Real World Evidence Expert
Carbon 60
SL1, ENG, GB
Full Time
Job DescriptionReal World Evidence (RWE) Expert Contract: Temporary - 6 months minimum Location: Slough (remote candidates also considered) Rate:...
Job Description
Real World Evidence (RWE) Expert Contract: Temporary - 6 months minimum Location: Slough (remote candidates also considered) Rate: (INSIDE IR35) - up to £40.38 per hour (PAYE) - up to £55.87 per hour (Umbrella) About the Role SRG are working with a leading pharmaceutical company who have an urgent contract need in their team. We are seeking an experienced Real World Evidence (RWE) Expert to lead the design, delivery and communication of global RWE projects. Working with a high degree of autonomy, you will manage studies from concept through to publication, generating evidence that informs healthcare decision-making, advances scientific understanding, and supports the development of real-world data capabilities. Key Responsibilities Design and deliver real-world evidence studies across areas such as epidemiology, natural history, burden of disease, care pathways, unmet need and real-world effectiveness. Develop study concepts, protocols and statistical analysis plans while ensuring quality, governance and milestone requirements are met. Lead secondary data studies and provide RWE expertise for primary data collection initiatives. Collaborate with academic partners, external vendors, medical experts, statisticians and analysts to deliver high-quality research. Interpret study findings and communicate insights effectively to internal and external stakeholders. Recommend appropriate methodologies and data sources, championing robust scientific approaches and evidence generation practices.Skills & Experience Required Proven experience delivering RWE projects using primary and/or secondary data within the pharmaceutical industry, consultancy, or academic research environment. Strong understanding of epidemiology, outcomes research and real-world study methodologies. Experience developing study protocols, statistical analysis plans and managing study governance requirements. Ability to work independently and manage multiple projects successfully to timelines and budget. Excellent stakeholder management and communication skills, with the confidence to influence and challenge appropriately. PhD in Epidemiology, Outcomes Research or a related discipline, plus experience in rare diseases, academic collaborations, or patient/carer-generated data, would be advantageous.To Apply Please click and submit your profile and/or to discuss further, contact Theo Charles on (phone number removed)Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy
This listing expired on 22 Jul. Applications are no longer accepted.
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