The Director, Real-World Biostatistics is a key role focused on advancing strategy and methodology in the entire course of drug/vaccine development using real-world data (RWD) within the enterprise. This position requires providing deep biostatistical expertise, strategic insight, and supporting methodological innovation to enhance the development and commercialization of pharmaceutical products, primarily in the oncology research unit (RU).
The Director will design and analyze RWD studies and other observational studies using cutting-edge biostatistical methodologies associated with causal inference and comparative effectiveness, clinical outcomes assessment, longitudinal and predictive modelling, and target trial emulation, while also mentoring staff assigned to these projects.
:
Biostatistical and Methodologic Support:
1. Lead and oversee the execution of real-world studies, ensuring methodological rigor, quality control, and regulatory adherence.
2. Create and refine statistical analysis plans, conduct complex statistical analyses, and convey findings to internal and external stakeholders.
3. Apply fit for purpose non-interventional statistical methods tailored to specific study objectives, ensuring robust data interpretation and insight generation.
Therapy Area Knowledge:
4. Develop in-depth knowledge on the assigned asset(s) and act as senior-level RWB consultant on matrix teams
Project Management and Staff Mentorship:
5. Mentor junior staff, guiding and developing their capabilities through mentorship, training, and professional growth opportunities while promoting knowledge sharing, continuous learning, and an innovative and collaborative environment.
6. Lead statistical efforts for assigned projects, manage timelines, resources, quality control, and coordinate across departments (e.g. epidemiology, health economics and outcomes research, clinical).
Communication and Strategic Initiatives:
7. Engage in strategic communication within the organization and with external audiences presenting statistical analyses and insights clearly and effectively at conferences, in publications, and during key stakeholder meetings, reinforcing the value of biostatistical contributions.
Methodological Development and Innovation:
8. Stay informed on industry trends, incorporate emerging biostatistical methods to enhance study designs and analytics, and participate in methodological research for the development of analytical techniques.
Regulatory Support and Compliance:
9. Provide biostatistical expertise on RWD during regulatory submissions, meeting preparations, and addressing queries to ensure alignment with regulatory standards while offering statistical guidance for organizational decision-making processes.
10. Stay informed with guidance documents from regulators to industry on use of RWD for regulatory decision-making
Basic Qualifications:
11. Ph.D. in Biostatistics, Statistics, Epidemiology or related disciplines with 8+ years (or Masters plus 10+ years) of working within the pharmaceutical/biotech industry (preferably in real-world evidence, epidemiology, or health outcomes functional areas)
12. Experience working with drug development processes and strategies, utilizing innovative statistical skills to meet project and/or business objectives
13. Experience leading pharmacoepidemiology and/or health outcomes analytics using RWD(e.g, electronic health record; insurance claims; registries) and applying observational study design and biostatistical principles to clinical/epidemiological research
14. Proficiency in programming languages (e.g., R, Python) and applied experience with observational data.
15. Experience in working according to regulatory requirements pertaining to RWD and clinical trials.
16. Experience in managing projects, delivering results in matrixed environments.
17. Experience in methodological research with contributions to publications in real-world data analytics.
Preferred Qualifications:
18. Experience in causal inference methodology such as propensity score based approaches, doubly-robust estimations including target maximum likelihood estimation (TMLE), principal stratification/instrumental variable approaches, methods for time-varying exposures.
19. Experience in time-to-event analysis in the setting of non-randomized studies
20. Experience in machine learning
21. Excellent communication and interpersonal skills for conveying complex statistical concepts effectively.
22. Fluency in written and spoken English
#LI-GSK
The annual base salary for new hires in this position ranges from $159,000 to $265,000 taking into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In 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.
Please visit to learn more about the comprehensive benefits program GSK offers US employees.
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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 we’re 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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