Study Manager – Real-World Evidence & Health Outcomes (Vaccines)
Location: Remote (Must be based in the UK)
Contract length - 9 Months
Pay rate: £826.31 umbrella rate
Join a large UK based Pharmaceutical manufacturer's Global Real-World Evidence (RWE) team to support the development and impact of our pneumococcal vaccine. In this role, you’ll design and deliver real-world and non-interventional studies that generate evidence to inform clinical, market access, and healthcare decision-making worldwide.
Key Responsibilities:
* Plan, design, and manage multiple RWE studies, ensuring quality, timelines, and budgets.
* Translate evidence needs into actionable study plans and insights.
* Collaborate across medical, R&D, and market access teams to align evidence generation.
* Advise on data sources and study design to meet global payer and HTA requirements.
* Communicate complex findings clearly to technical and non-technical audiences.
About You:
* MSc (or equivalent) in health outcomes, epidemiology, health economics, pharmacy, or life sciences.
* 5+ years’ experience in pharma, ideally with RWE or health outcomes research.
* Strong project management and cross-functional collaboration skills.
* Confident communicator who can translate data into meaningful insights.
* Experience with pneumococcal is highly advantageous
Desirable: PhD/PharmD, global or payer experience, and product launch exposure.
If you’re passionate about generating evidence that shapes healthcare decisions and improves patient outcomes, we’d love to hear from you.