Associate Director, Global Epidemiology and Real-World Evidence

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Associate Director Global Epidemiology and Real-World Evidence

Join GSK as an Associate Director Global Epidemiology and Real-World Evidence and lead epidemiology efforts that shape evidence across development and lifecycle activities. You will work with clinical development safety regulatory outcomes and commercial partners. You will design and deliver epidemiologic studies using real-world data registries and other sources. We value clear thinkers who communicate well solve practical problems and put patients first. This role offers growth visible impact on decisions that matter for patients and a chance to help unite science technology and talent to get ahead of disease together.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• Lead epidemiology programs for one or more assets or disease areas creating strategy and timelines with cross-functional partners.
• Design oversee and deliver observational and database studies using real-world data registries and linked sources.
• Provide timely scientific advice on study design data needs analysis plans and interpretation of results to asset teams.
• Manage external partners vendors budgets and timelines to ensure high-quality on-time study delivery.
• Prepare regulatory documents technical reports and publications that clearly communicate study findings.
• Build capability by sharing methods best practice and learnings across teams.

Basic Qualifications & Skills:

We are looking for professionals with these required skills to achieve our goals:

• Masters degree in Epidemiology Public Health Biostatistics or a related quantitative discipline. Doctoral degree acceptable.
• Minimum 5 years of applied epidemiology pharmacoepidemiology outcomes research or related experience.
• Proven experience designing and delivering observational studies or healthcare database analyses.
• Experience working in a matrix environment and collaborating with clinical safety regulatory or outcomes teams.

Preferred Qualifications & Skills:

Please note the following skills are not necessary just preferred if you do not have them please still apply:

• PhD in Epidemiology Public Health Biostatistics or a related field.
• Experience in industry supporting regulatory submissions post-authorization commitments or safety assessments.
• Familiarity with multiple real-world data types (electronic health records claims registries) and data linkage.
• Knowledge of advanced quantitative methods such as causal inference target trial emulation or propensity-based approaches.
• Record of peer-reviewed publications and presentations at scientific meetings.
• Experience engaging with regulators advisory boards or external scientific networks.
• Strong written and verbal communication skills able to explain methods to technical and non-technical audiences.

This role is based in the United States and offers a hybrid working environment with a blend of remote and onsite collaboration. Presence in the office is expected to be approximately 2-3 days per week to engage with colleagues and stakeholders.

If you want to develop your expertise in epidemiology and help deliver new medicines that improve lives we encourage you to apply. Join us in a welcoming and inclusive environment where your ideas and skills will help shape the future of healthcare. Together we get ahead of disease.

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Skills

Business Acumen Drug Development Pharmacoepidemiology Real World Data Real World Evidence (RWE) Strategic Influence

If you are based in Cambridge MA; Waltham MA; Rockville MD; or San Francisco CA the annual base salary for new hires in this position ranges $149325 to $248875. The US salary ranges take into account a number of factors including work location within the US market the candidates skills experience education level and the market rate for the addition this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family) retirement benefits paid holidays vacation and paid caregiver/parental and medical leave. If salary ranges are not displayed in the job posting for a specific country the relevant compensation will be discussed during the recruitment process.

Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

Why GSK

Uniting science technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade as a successful growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory immunology and inflammation; oncology; HIV; and infectious diseases to impact health at scale.

People and patients around the world count on the medicines and vaccines we make so were committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients accountable for impact and doing the right thing is the foundation for how together we deliver for patients shareholders and our people.

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