VP, Head of Clinical Sciences, Vaccines and Infectious Disease

Job description

Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together. Find out more: Our approach to R&D Position Summary As VP, Head of Clinical Sciences, Vaccines and Infectious Diseases, you provide clinical leadership across a high-impact global portfolio, shaping clinical strategy, overseeing medical and scientific governance, and ensuring strong benefit–risk decisions for people in our studies. You lead and mentor clinical teams, building capability and creating an inclusive environment that supports growth and innovation. Driving excellence in clinical development plans and study designs, you help deliver high-quality evidence from early research to life cycle management, collaborating closely with internal partners to integrate patient, physician, and payer insights into development and evidence strategies. This is a senior role for a proven clinical leader who brings deep vaccines expertise, strategic thinking, and a passion for impact at scale Responsibilities Provide senior clinical leadership and strategy for the Vaccines and Infectious Diseases portfolio, across early and late development stages. Act as the single point of clinical and medical leadership for the portfolio, guiding development and commercial teams with clear insight. Ensure clinical input to regulatory documents and interactions is accurate, scientifically robust, and delivered on time. Provide globally integrated clinical and medical governance of studies, ensuring scientific integrity and appropriate benefit–risk for participants. Manage and allocate clinical staff and resources across programs, aligning resourcing with portfolio priorities and agreed plans. Lead project oversight to secure timely, efficient, and compliant delivery of clinical activities and enhance end-to-end pipeline productivity. Drive innovation in clinical development, including simplified approaches, outsourced study models, and question-based trial designs where appropriate. Embed Clinical Trial Representativeness principles across the program to support more inclusive and relevant evidence generation. Strengthen cross-functional collaboration, integrating patient, physician, and payer perspectives and working with medical and epidemiology leaders on evidence plans. Lead talent management for clinical sciences, including recruitment, development, succession planning, and promotion of equity and inclusion. Sponsor the Global Clinical Community, supporting peer review and forums that share learning and best practice. Identify, assess, and mitigate risks across the scope of Vaccines and Infectious Diseases Clinical Sciences work. Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals: Medical Doctor or PhD, with deep experience in vaccines or drug development and strong therapy area expertise. At least 15 years’ experience in vaccines development, covering multiple stages of clinical research and development. A minimum of 5+ years’ experience leading medical experts in academia or industry, with responsibility for teams and complex programs. Proven experience designing, conducting, interpreting, and reporting high-quality clinical studies, in line with Good Clinical Practice and internal controls. Experience providing clinical judgment and governance for late-stage programs and life cycle management activities. Preferred Qualification If you have the following characteristics, it would be a plus: Strong leadership capability, with a track record of inspiring teams, mentoring individuals, and allocating resources strategically. Advanced strategic thinking skills, able to balance complex issues and competing priorities and develop effective clinical and portfolio strategies. Business acumen, including understanding how clinical and resource decisions affect business outcomes and the wider organization. Project management experience using risk-based planning to deliver projects to agreed timelines and quality standards. In-depth scientific and medical knowledge of relevant vaccines, therapeutic and disease areas, and associated evidence needs. Experience in medical monitoring and pharmacovigilance, including appropriate escalation to specialist safety functions when needed. Understanding of reimbursement and market access considerations and the evidence required to support payer value and vaccine recommendations. Strong scientific writing skills, producing clear, accurate, and rigorous scientific communications in line with internal standards. Confident scientific presentation skills, able to communicate with credibility to internal and external stakeholders and experts. Why You? This role is hybrid with regular on-site presence in Belgium, Italy or US. We seek a hands-on leader who is motivated by scientific challenge and patient impact. You will join a supportive environment where collaboration and inclusion shape how we work. How to apply If this role speaks to you, we encourage you to apply. Tell us how your experience and leadership will help shape clinical programs that make a real difference to patients and public health. We look forward to hearing from you. Skills Analytical Thinking, Business Strategies, Clinical Development, Clinical Research, Clinical Trial Designs, Communication, Decision Making, Fostering Collaboration, Influencing Without Authority, Leadership, People Management, Risk Management, Strategic Thinking, Strategy Development, Teamwork • 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 $315,750 to $526,250. The US salary ranges take 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. If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.Italian Salary Range / Fascia retributiva in Italia: EUR 0 to EUR 0Belgium Salary Range / Fourchette salariale – Belgique: EUR 236,250 to EUR 393,750The annual gross base salary range for new hires in this position is listed above for each applicable location. These ranges take into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role. In addition, this position may offer an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. More detailed information on the total benefits package will be supplied during the recruitment process. This role is available for applicants from multiple locations, and therefore salary ranges for certain locations are also shown. Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salar