Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology
GSK · 6 Locations · GB
Medical Affairs
–
Not yet analysed
Demand78
Career growth80
Healthcare fit74
Remote potential45
5-year outlook
Director-level pharma RWE/HEOR roles sit in a well-compensated, structurally growing function as payers and regulators demand real-world value evidence; expect competitive senior pharma compensation with steady upward trajectory, though exact figures vary by country and band.
Clinical license
Not required
Applicant reach
narrow
Seniority
lead
Employment type
–
Date found
2026-10-20
Intelligence details
Flexible work details
- Eligible countries
- United Kingdom
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth considering only if you are an oncology clinician who already has outcomes research, epidemiology, or pharma medical affairs experience — the title signals a senior strategic leadership post, not a transition entry point.
Who should apply
Oncology physicians or clinical pharmacists with HEOR, epidemiology, or real-world evidence experience; clinician-scientists with observational study and publication track records; former medical affairs or evidence-generation leads in pharma or CROs.
CV angle
Foreground genuine oncology clinical depth (tumour types, treatment pathways, trial involvement) and translate it into evidence language: study design, endpoint selection, real-world data sources (EHR, claims, registries), patient-reported outcomes, and publication/scientific communication. Quantify cross-functional leadership, protocol contributions, and any HTA/payer-facing or regulatory-grade evidence work — do not claim HEOR or pharma experience you do not have.
Skills to highlight
- Oncology clinical expertise
- Observational/real-world study design and epidemiology
- Real-world data sources (EHR, claims, registries)
- Health outcomes and patient-reported outcomes measurement
- Scientific writing and publication
- Cross-functional and vendor leadership
- Regulatory and HTA evidence awareness
Role summary
A senior pharma role leading global real-world evidence and health outcomes strategy across an oncology portfolio — designing observational studies, shaping evidence generation plans, and translating real-world data into value and access messages for regulators, payers, and clinicians.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.