Director, US Real-World Evidence – Health Outcomes

GSK

GSK biopharma evidence director leading US oncology real-world evidence and health outcomes research. Developing studies and evidence plans supporting product positioning, pricing, and commercialization decisions.

Posted 8/5/2026full-timePhiladelphia • North Carolina, Pennsylvania • 🇺🇸 United StatesLeadWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Real-World Evidence (RWE) and Health Outcomes research, with a strong background in study design, statistical analysis, and project management within the pharmaceutical industry. Capable of leading cross-functional teams and managing vendor relationships to ensure successful evidence generation and compliance with regulatory standards.

Highest-signal resume keywords

Real-World Evidence ExpertiseHealth Outcomes ResearchProject ManagementStatistical Analysis PlansCommunication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Health EconomicsEpidemiologyBiostatisticsStudy DesignData-Source SelectionBias MitigationPublication PlanningStatistical AnalysisResearch ProtocolsEconomic Evaluation

Soft Skills

Strong CommunicationPresentation SkillsPrioritizationAdaptabilityRelationship Building

Certifications & Qualifications

Master’s DegreePhD

Industry Keywords

Pharmaceutical IndustryOncologyReal-World EvidenceHealth OutcomesClinical Congresses

About the role

Key responsibilities & impact

Develop and deliver components of the US data generation plan, including real-world evidence and economic value evidence
Develop evidence generation plans, study concepts, protocols, workplans, timelines, and resourcing proposals
Lead assigned real-world evidence and health outcomes studies, including design and execution with internal functions and external vendors
Provide periodic reporting and keep key stakeholders updated on study plans
Build relationships with external thought leaders and ensure appropriate research methods and agendas
Manage cross-functional alignment across medical, market access, R&D, and commercial stakeholders
Lead meetings on evidence-generation gaps and priorities
Draft and review project specifications, protocols, statistical analysis plans, study reports, abstracts, posters, and manuscripts
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, contractors, study scope, timelines, budgets, and change control
Complete required training, follow SOPs, and contribute to process improvement

Requirements

What you’ll need

Master’s degree or PhD in health economics and outcomes research, epidemiology, public health, biostatistics, or a related discipline
3+ years’ experience within the pharmaceutical industry or academia-related research within US Oncology
Experience designing publication plans and presenting RWE/HO research at major clinical congresses
Experience managing multiple projects simultaneously
Expertise in real-world evidence and economic evaluation study designs and methods
Experience developing research questions, endpoints, data-source selections, and bias/confounding mitigation approaches
Experience reviewing or authoring statistical analysis plans and study reports
Experience ensuring publication and disclosure readiness in accordance with internal SOPs and external requirements
Strong communication and presentation skills
Ability to prioritize, pivot, and manage multiple projects in a matrix environment

Benefits

Comp & perks

Comprehensive benefits program for US employees
Support for employee wellbeing
Opportunities for growth and development
Accommodation or other assistance to apply, if required