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A global biopharmaceutical company is seeking a Senior Manager in Outcomes & Evidence to lead the evidence generation for market access in the UK. The role involves developing strategies to address evidence gaps for pre‑marketed medicines. Candidates must have experience in real-world evidence and HTA processes, with excellent project management and interpersonal skills. A hybrid work model is offered.
Our focus is on patients and understanding the critical role our medicines play to produce better patient outcomes. Access and Value is a cross‑functional team of experts who create and execute comprehensive market access strategies through the integration of access policy shaping and stakeholder engagement, pricing and reimbursement, evidence generation and health economic modelling activities. Your expertise and innovative approaches will help us to better demonstrate the value of our medicines and their impact on patient outcomes.
You will be part of Pfizer’s dynamic market access, Access & Value UK, team and will have the important role of evaluating and delivering on the evidence needs for pre‑marketed medicines in the UK. A&V comprises three sub‑teams – Health Technology Assessment (HTA), Asset & Access (A&A) and Outcomes & Evidence (O&E). This role sits in the O&E team who lead the evidence generation needs to support reimbursement and access in the UK.
In this role, the primary function is to lead an optimised evidence strategy for the UK’s HTA submissions. This requires the individual to identify gaps in evidence, prioritise those which will make a difference to the likelihood of reimbursement and, if required, plan and deliver new real‑world evidence (RWE) studies (such as treatment patterns and healthcare resource use). To achieve this, the individual works hand‑in‑hand with HTA and A&A to drive the overall reimbursement and access strategy which requires strong cross‑functional engagement to ensure the strategies are aligned with the UK launch and wider Global strategies.
We are seeking an individual who can demonstrate experience in leading RWE studies in the UK and provide scientific input into designs and methods that will ensure the robustness and credibility of the results by NICE/JCVI. In addition, they will need to understand the HTA process and adopt a high‑level understanding of cost‑effectiveness modelling to assess how new evidence can influence the economic value of our medicines and vaccines. They will be managing multiple pipeline assets and will therefore need excellent time management and prioritisation skills. Strong interpersonal skills to positively collaborate with multiple internal stakeholders and key external stakeholders will also be required to ensure that our work is comprehensive and valuable to patients as well as the UK business.
Work Location Assignment:Hybrid
Equal Employment Opportunity