Director, Global Real-World Evidence – Health Outcomes Scientist, Oncology

This is a fully remote position, open to applicants in United States, +3 more locations.

📋 Description

• Strategize, design, and implement various studies for a specific asset.

• Oversee study timelines, deliverables, and budget management.

• Ensure quality of deliverables and review/sign off on project specifications, protocols, data analysis plans, final study reports, abstracts, posters, and manuscripts in compliance with SOPs.

• Identify necessary resources, references, and analyses to guide scientific design.

• Provide advice to internal and external experts supporting the asset team.

• Convert evidence requirements into study concepts that align with strategic objectives.

• Create innovative and cost-efficient methods for study development and execution.

• Stay informed about real-world data resources, partnerships, and public initiatives.

• Advise on the suitability of data sources for research inquiries.

• Cultivate an understanding of customer needs, clinician requirements, HTA criteria, and evidence acceptance.

• Collaborate with internal teams and engage in best-practice sharing sessions.

• Foster relationships across medical, market access, R&D, and commercial teams.

• Ensure strategic alignment and encourage cross-functional collaboration.

• Regularly inform key stakeholders and business leaders through periodic updates.

• Build rapport with external thought leaders and ensure appropriate methods and research agendas are applied in accordance with GSK policies.

⛳️ Requirements

• MSc or equivalent in health outcomes, health economics, epidemiology, pharmacy, health, or life sciences.

• Over 3 years of experience in the pharmaceutical industry, preferably within a multinational company.

• Experience in Oncology or Hematology.

• Proven track record in planning and delivering individual projects, managing budgets, and operating within a matrix environment.

• Background in designing RWE studies, including prospective observational studies, cross-sectional and retrospective cohort studies, chart reviews, and database analyses.

• Proficient in utilizing evidence for HTA submissions, reimbursement, and/or medical engagements.

• Demonstrated history of providing robust payer evidence and engaging meaningfully with external experts and leaders.

• In-depth knowledge of healthcare markets, health technology assessment agencies, and reimbursement decision-making on a global scale, as well as in regional and local markets.

• Experience in communicating technical and complex concepts and results to diverse audiences to influence decision-making.

• Preferred: advanced scientific degree, such as PhD, PharmD, or equivalent.

• Preferred: experience in prostate cancer.

• Preferred: experience in global and country oncology roles.

• Preferred: experience with product launches.

🏝️ Benefits

• Competitive salary.

• Annual bonus based on company performance.

• Healthcare and wellbeing programs.

• Pension plan membership.

• Shares and savings program.

• Remote or hybrid working model.

• Health care and other insurance benefits for employees and their families.

• Retirement benefits.

• Paid holidays.

• Vacation.

• Paid caregiver/parental and medical leave.

• Eligibility for share-based long-term incentive programs.