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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in developing and implementing real-world evidence and health outcomes research plans, with a strong focus on oncology and economic evaluation methodologies. Proven ability to manage multiple projects, collaborate with cross-functional teams, and ensure compliance with research standards.
Highest-signal resume keywords
Real-World Evidence (RWE) ResearchHealth Outcomes ResearchOncology ExperienceProject ManagementStatistical Analysis Plans
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Health EconomicsEpidemiologyBiostatisticsCost-Effectiveness AnalysisBurden-of-Illness StudiesTreatment-Pattern AnalysisData Source SelectionBias MitigationPublication PlanningStudy Protocol Development
Soft Skills
Strong Communication SkillsPresentation SkillsAbility to Influence Without AuthorityCollaborationPrioritization
Tools & Technologies
EHRClaims DataRegistries
Industry Keywords
Pharmaceutical IndustryManaged CareHealthcare ConsultingClinical CongressesStakeholder Engagement
About the role
Key responsibilities & impact- Develop and implement US real-world evidence and health outcomes research plans
- Design multiple RWE/HO studies aligned with US medical, payer, and access needs
- Translate evidence strategy into actionable workplans, timelines, and resourcing proposals
- Develop study concepts, protocols, and innovative, cost-effective study execution approaches
- Lead day-to-day delivery of assigned RWE and health outcomes studies
- Manage real-world evidence studies, cost-effectiveness and budget-impact analyses, burden-of-illness studies, treatment-pattern analyses, and patient-focused outcomes research
- Partner with internal functions and external vendors on study design and execution
- Provide periodic updates to key stakeholders and business leaders
- Build relationships with external thought leaders and ensure compliant research methods and agendas
- Collaborate with medical, market access, R&D, and commercial stakeholder groups
- Lead cross-functional meetings on evidence gaps and priorities
- Draft and review project specifications, protocols, statistical analysis plans, study reports, abstracts, posters, and manuscripts
- Ensure scientific, operational, SOP, governance, and compliance quality
- Provide RWE and health outcomes input for development and commercialization decisions
- Gather customer insights from Field Based Payer Medical Teams and other field stakeholders
- Manage vendors and contractors, including scope, timelines, budgets, and change control
- Escalate risks and issues proactively
- Contribute to continuous improvement of RWE and health outcomes processes
Requirements
What you’ll need- Master’s degree or PhD in health economics and outcomes research, epidemiology, public health, biostatistics, or related discipline
- 5+ years’ experience within the pharmaceutical industry or academia related research within US Oncology experience
- Experience designing a publication plan and having a presence of RWE/HO research studies at major clinical congresses
- Experience managing multiple projects simultaneously
- Experience in RWE and economic evaluation study designs/methods, evidenced by publications and/or contributing to study concept sheets and protocols
- Experience with clear research questions, endpoints, data source selection, and bias/confounding mitigation
- Experience reviewing/authoring key sections of statistical analysis plans and study reports
- Experience ensuring publication/disclosure readiness in accordance with internal SOPs and external requirements
- Preferred: demonstrated success developing and executing health outcomes research plans and delivering high-quality data generation outputs
- Preferred: oncology (NSCLC) experience, including familiarity with evolving standards of care, evidence requirements, and stakeholder needs
- Preferred: Master’s plus approximately 4–6 years or PhD with 2–4+ years of experience in pharmaceutical industry and/or managed care, hospital, academic, or healthcare consulting environments
- Preferred: experience collaborating with field-facing teams and/or Market Access partners
- Preferred: experience managing real-world data sources and vendors, including claims, EHR, and registries
- Preferred: ability to influence without authority in a matrix environment
- Preferred: strong communication and presentation skills
- Preferred: ability to prioritize, pivot, and manage multiple projects simultaneously
- Preferred: strategic execution experience translating evidence strategy into workplans and delivering outputs across 1–2 concurrent asset workstreams
- Preferred: project and vendor management experience, including scope, success criteria, budgets, timelines, risks/issues, and change control
- Preferred: experience contributing to congress strategy and publication planning
- Must complete required training and adhere to company/department SOPs
Benefits
Comp & perks- Comprehensive benefits program for US employees (details provided in GSK US Benefits Summary)
- Equal Opportunity Employer