Real World Evidence Expert

The successful candidate will play a key role in a variety of rare disease research programmes with a focus on delivering regulatory studies.

Key Responsibilities

• Lead the design, execution, and delivery of global RWE studies from concept through to publication.
• Develop study concepts, protocols, statistical analysis plans, and project documentation.
• Deliver studies on time and within budget while ensuring compliance with governance and quality requirements.
• Support and advise local study teams on methodology, project delivery, and operational challenges.
• Represent RWE expertise within primary data collection studies.
• Collaborate with academic research groups, external vendors, medical experts, statisticians, and analysts.
• Interpret study findings and communicate results to both internal and external stakeholders.

Essential Experience

• Minimum 3 years RWE experience, delivering real-world evidence projects using primary and secondary data
• Experience gained within the pharmaceutical industry, a leading consultancy, or a recognised academic centre of excellence
• Strong project management and ability to collaborate effectively with clinicians or key opinion leaders

Desirable Experience

• PhD in Epidemiology, Outcomes Research, or a related discipline
• Experience working with patient- or carer-reported data
• Experience within fertility, preterm birth, obstetric illnesses, pregnancy, lactation or neonatal health

The jobholder can either work exclusively from home or on a hybrid basis. This role is offered on an initial 12 month contract with opportunity for extension.

Keywords: pharmaceutical, clinical trials, real world evidence, RWE, epidemiology, health science, outcomes research, Slough, London, Oxford, Reading, VRS9561SE