CareerAddict

Real World Evidence Expert

CV-Library

Posted on Jul 10, 2026 by CV-Library
Slough, Berkshire, United Kingdom
Pharmaceutical
Immediate Start
£34 - £40.6 Hourly
Temporary
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

Reference: 225356161

https://jobs.careeraddict.com/post/113540959
CV-Library

Real World Evidence Expert

CV-Library

Posted on Jul 10, 2026 by CV-Library

Print
Slough, Berkshire, United Kingdom
Pharmaceutical
Immediate Start
£34 - £40.6 Hourly
Temporary
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
Print

Reference: 225356161

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