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Epidemiologist – Global RWE & Health Outcomes Research CV-Library Epidemiologist - Global RWE &[...]

Scienceabode

United Kingdom

Hybrid

GBP 80,000 - 100,000

Full time

Today
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Job summary

A leading global pharmaceutical organization seeks a Global RWE & Health Outcomes Research Analyst to support evidence generation strategies. Your role will involve collaborating across functions, managing data generation plans, and overseeing non-interventional studies. Candidates should have an MSc in relevant fields and experience in the pharmaceutical industry. This position offers a chance to contribute to significant projects in a high-visibility environment.

Qualifications

  • Experience within the pharmaceutical or biotechnology industry.
  • Practical experience delivering RWE and/or non-interventional studies.
  • Familiarity with regulatory, HTA, or payer evidence expectations.

Responsibilities

  • Support asset-level RWE and HEOR strategy.
  • Design, execute, and oversee non-interventional studies.
  • Collaborate with internal stakeholders.

Skills

Stakeholder management
Scientific communication
Cross-functional collaboration

Education

MSc in Health Outcomes Research
MSc in Health Economics
MSc in Epidemiology
Job description
Global RWE & Health Outcomes Research Analyst

Location: Homebased / Hybrid

Sector: Pharmaceutical / Biotechnology

CY Partners is partnering with a leading global pharmaceutical organisation to recruit a Global Real-World Evidence (RWE) & Health Outcomes Research (HOR) Analyst / Epidemiologist. This role sits within a mature, globally integrated RWE & HOR function and supports a strategic, late-stage / marketed priority asset across its lifecycle.

This opportunity is well suited to candidates with hands‑on experience working in, or closely with, the pharmaceutical industry, who are looking to deepen their impact in global evidence generation.

The Role

Reporting directly to the Global RWE & HOR Lead, you will contribute to the development and execution of asset‑level real‑world evidence strategies aligned to regulatory, access, and medical needs. You will work cross‑functionally within a complex global matrix, collaborating closely with Medical Affairs, HEOR, Clinical Development, Market Access, and external research partners.

Key Responsibilities
  • Support asset‑level RWE and HEOR strategy across development and/or lifecycle management
  • Contribute to the planning and delivery of Data Generation Plans (DGPs) aligned to regulatory, HTA, and payer evidence requirements
  • Design, execute, and oversee non‑interventional studies (e.g. observational studies, registries, database studies)
  • Collaborate with internal stakeholders including Global Medical Affairs, HEOR, Market Access, Clinical, Biostatistics, and Regulatory
  • Manage and engage with external vendors, CROs, data owners, and academic collaborators
  • Support interpretation, scientific validation, and dissemination of RWE outputs (e.g. congresses, publications, internal decision‑making)
  • Ensure studies meet internal governance, quality, and compliance standards typical of a global pharmaceutical organisation
Candidate Profile

MSc (or equivalent) in a relevant discipline, such as:

  • Health Outcomes Research
  • Health Economics
  • Epidemiology
  • Patient‑Reported Outcomes
  • Pharmacy
  • Health or Life Sciences

Demonstrable experience within the pharmaceutical or biotechnology industry, or in a consultancy/CRO supporting pharma clients

Practical experience delivering RWE and/or non‑interventional studies in an industry setting

Familiarity with regulatory, HTA, or payer evidence expectations

Strong ability to operate within global, cross‑functional matrix teams

Excellent stakeholder management and scientific communication skills

Why Apply?

This is an opportunity to work on a high‑visibility global asset, contribute to evidence that directly informs regulatory, access, and medical strategy, and grow your career within a best‑in‑class pharmaceutical RWE & HEOR function.

For more information or a confidential discussion, please contact CY Partners

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