Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology
GSK
full-time
Posted on:
Location Type: Hybrid
Location: Upper Providence • Pennsylvania • United States
Visit company websiteExplore more
Salary
💰 $204,000 - $340,000 per year
Job Level
About the role
- Plan, design and execute multiple studies for a given asset and manage timelines, deliverables, and budget
- Assure quality of deliverables, including review and sign off project specifications, protocols, data analysis plans, final study reports, abstracts, posters and manuscripts, in adherence to SOPs
- Identify resources, references and analyses to inform scientific design and advise internal experts (medical affairs, clinical, commercial/market access) and external experts as needed in support of the asset team
- Translate needs for evidence into study concepts in alignment with strategic objectives and vision for the asset, e.g. development of study protocols and proposing innovative and cost-effective ways of developing and executing studies
- Develop and maintain a good working knowledge of real-world data resources, existing partnerships and public initiatives and become the point person for select sources to advise on their suitability to address given research questions
- Develop a deep understanding of customers’ needs, including clinicians and HTA requirements, and their acceptance of different types of evidence and impact of that evidence to their decision making
- Collaborate with internal teams and participate in best practice sharing sessions across the non-interventional study organization
- Build strong working relationships with stakeholder groups across medical, market access, R&D and commercial to ensure strategic alignment and optimal cross-functional collaboration and communication
- Ensure key stakeholders, including TA aligned business leaders, are regularly updated on plans through periodic reporting
- Develop excellent working relationships with external thought leaders to 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
- 3+ years of experience working in the pharmaceutical industry, preferably in a multi-national company
- Experience in planning and delivering individual projects, managing budgets and working within a matrix setting
- A history of designing a variety of RWE studies including prospective observational studies, cross-sectional and retrospective cohort studies, chart reviews, and database analyses
- Proficiency in utilizing evidence for the development of HTA submissions, reimbursement and/or medical engagements
- A track record of delivering robust payer evidence and credibility to engage meaningfully with external experts and leaders in the field
- Expertise with the diversity and complexity of healthcare markets, health technology assessment agencies, and reimbursement decision making globally, in region and local markets
- Experience in communicating technical and complex concepts and results to various audiences to impact decision-making
- Experience in Oncology or Hematology
Benefits
- health care and other insurance benefits (for employee and family)
- retirement benefits
- paid holidays
- vacation
- paid caregiver/parental and medical leave
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
health outcomeshealth economicsepidemiologypharmacyreal-world evidence (RWE)HTA submissionsprospective observational studiescross-sectional studiesretrospective cohort studiesdatabase analyses
Soft Skills
project managementbudget managementcross-functional collaborationcommunicationrelationship buildingstakeholder engagementstrategic alignmentproblem-solvingadaptabilityteamwork
Certifications
MSc in health outcomesMSc in health economicsMSc in epidemiologyMSc in pharmacyMSc in health sciencesMSc in life sciences