Associate Director, Real World Evidence
GSK
6 hours ago
Remote friendly (Collegeville, PA)
United States
Clinical Research and Development
Associate Director, Real World Evidence
You will lead real world evidence work that shapes how vaccines demonstrate benefit to patients, health systems and payers globally. You will work closely with cross-functional teams including Medical Affairs, Market Access, R&D, Commercial and external partners.
In this role you will provide YOU the opportunity to lead key activities:
- Lead the development and delivery of real world evidence plans to support medical strategy, product access, pricing and life-cycle decisions.
- Work with cross-functional teams to translate evidence needs into study designs, data collection and analysis plans.
- Represent the team in external engagements, including scientific conferences, payers, health technology assessment agencies, clinical stakeholders and scientific partners.
- Drive dissemination of outcomes evidence through value dossiers, scientific reports, publications and internal training.
- Ensure data generation plans and study outputs align with medical strategy and commercial needs through cross-functional alignment and decision making.
Basic Qualifications & Skills (required):
- Advanced degree (MSc, MPH, MSc Health Economics, PhD or equivalent) in health economics, epidemiology, statistics, public health or a related field.
- Demonstrated experience in public health research, clinical trials, health economics, outcomes research, real-world evidence or market access in the pharmaceutical, academic, or consulting sector.
- Practical experience engaging with NITAGs, payers and/or policy decision makers.
- Strong written and verbal communication skills, producing technical reports and value dossiers.
- Ability to work effectively in a cross-functional matrix and manage external vendors or academic collaborators.
- Expertise developing scientific collaboration with external stakeholders, leading cross-functional research teams, and coordinating complex projects.
Preferred Qualifications & Skills:
- PhD or MSc with substantial experience in health economics or outcomes research.
- Hands-on programming skills in R, Excel modelling expertise, or familiarity with health economic modelling software.
- Experience with real-world evidence study design (e.g., pragmatic RCTs, database analyses, health economic modelling).
- Vaccine research experience.
- Ability to apply Scientific Engagement principles to complex, unique situations.
- Excellent communication/presentation/listening skills in a multicultural matrix organization.
Closing Date for Applications: 28th April 2026
Application instructions:
- Use the online application cover letter or your CV to describe how you meet the competencies outlined in the job requirements.
You will lead real world evidence work that shapes how vaccines demonstrate benefit to patients, health systems and payers globally. You will work closely with cross-functional teams including Medical Affairs, Market Access, R&D, Commercial and external partners.
In this role you will provide YOU the opportunity to lead key activities:
- Lead the development and delivery of real world evidence plans to support medical strategy, product access, pricing and life-cycle decisions.
- Work with cross-functional teams to translate evidence needs into study designs, data collection and analysis plans.
- Represent the team in external engagements, including scientific conferences, payers, health technology assessment agencies, clinical stakeholders and scientific partners.
- Drive dissemination of outcomes evidence through value dossiers, scientific reports, publications and internal training.
- Ensure data generation plans and study outputs align with medical strategy and commercial needs through cross-functional alignment and decision making.
Basic Qualifications & Skills (required):
- Advanced degree (MSc, MPH, MSc Health Economics, PhD or equivalent) in health economics, epidemiology, statistics, public health or a related field.
- Demonstrated experience in public health research, clinical trials, health economics, outcomes research, real-world evidence or market access in the pharmaceutical, academic, or consulting sector.
- Practical experience engaging with NITAGs, payers and/or policy decision makers.
- Strong written and verbal communication skills, producing technical reports and value dossiers.
- Ability to work effectively in a cross-functional matrix and manage external vendors or academic collaborators.
- Expertise developing scientific collaboration with external stakeholders, leading cross-functional research teams, and coordinating complex projects.
Preferred Qualifications & Skills:
- PhD or MSc with substantial experience in health economics or outcomes research.
- Hands-on programming skills in R, Excel modelling expertise, or familiarity with health economic modelling software.
- Experience with real-world evidence study design (e.g., pragmatic RCTs, database analyses, health economic modelling).
- Vaccine research experience.
- Ability to apply Scientific Engagement principles to complex, unique situations.
- Excellent communication/presentation/listening skills in a multicultural matrix organization.
Closing Date for Applications: 28th April 2026
Application instructions:
- Use the online application cover letter or your CV to describe how you meet the competencies outlined in the job requirements.