Description

Job description
Site Name: 200 CambridgePark Drive, Belgium-Wavre, GSK HQ, Italy - Siena, USA - Maryland - Rockville
Posted Date: Jun 4 2026

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

The Vaccines/Infectious Diseases (Vx/ID) Cluster Head is a core member of the Vx/ID Diseases Clinical Science Leadership Team and acts as the single point of accountability for the integrated Clinical Development Plan (CDP), contributing to the disease area strategy with input from both internal GSK leaders and external experts, including academic thought leaders and regulatory authorities. This role is responsible for ensuring the delivery of robust CDPs that explore new areas of interest and alternative development pathways, enabling smart risk-taking for assets within the disease area.

 

The Vx/ID Clinical Science Cluster Head drives innovation in the design of CDPs and study protocols, accessing world-class expertise through collaboration and harnessing digital, technological, and statistical tools to support all development stages. They provide Clinical/Medical Governance, managing and mentoring clinical staff, ensuring proper training and compliance, and fostering Clinical Development Excellence through talent identification, recruitment, and retention. Additionally, this role ensures the quality of all clinical deliverables, including documents, submissions, and clinical data, through peer review and knowledge sharing, and oversees high-quality presentations to regulatory bodies. The Vx/ID Clinical Sciences Cluster Head also acts as a Data Steward for the disease area, manages resources across clinical projects, and leads project oversight to ensure timely delivery of clinical programs.

Responsibilities

Clinical Development

• Accountable for the clinical development planning of assets within their disease area, ensuring alignment with key clinical stakeholders and providing clinical/medical overview over the CDP.
• Lead interpretation and critical evaluation of study results with respective clinical development leaders.

Disease Expert Input and Resource Allocation

• Accountable for allocating appropriate disease expert input to the appropriate Project Team (e.g. Vaccine Development Team) to support the delivery of Vaccines target profiles.
• Manage and allocate clinical personnel across projects and programs within the disease area portfolio, ensuring appropriate resourcing.

Disease Area Strategy

• Accountable to work with the Head of Clinical Sciences to set forward the disease area strategy for clinical development, ensuring it is informed by world-class expertise and aligned with business goals.
• Lead the external scientific insight strategy for the disease area, incorporating input from scientific experts, patients, physicians, payers, and regulators.

Regulatory and Scientific Integrity

• Accountable for the accuracy and scientific integrity of clinical input to regulatory documents and meetings with global impact, overseeing asset-level Clinical Development Leaders.
• Ensure the delivery of high-quality regulatory documentation and packages to support desired indications.

Medical Governance

• Accountable for providing globally integrated medical governance of clinical research, ensuring scientific integrity and overall safety of study subjects.
• Support interactions with Medical Affairs and Global Clinical Safety and Pharmacovigilance leaders to maintain robust medical governance.

Pipeline Productivity and Simplification

• Enhance delivery and improve end-to-end pipeline productivity by driving clear disease area strategies, aligned Vaccine product profiles, and Clinical Development Plans.
• Drive simplification and reduce complexity across R&D, exploring opportunities for optimal resourcing models and risk mitigation.

Organizational Decision-Making

• Enhance organizational decision-making by supporting optimal project-level decisions, promoting innovative trial designs, and considering alternative development pathways for smart risk-taking.
• Embed Clinical Trial Representativeness principles throughout the clinical development program.

R&D Commercial Interface

• Improve the R&D Commercial interface by ensuring that patient, physician, and payer insights are incorporated for all clinical-stage assets.
• Foster collaboration to strengthen evidence generation plans and portfolio delivery beyond market authorization approval.

Talent Management and Leadership Development

• Accountable for robust talent management, focusing on improving leadership across clinical members through mentoring, coaching, and succession planning.
• Ensure inclusion and participate in peer reviews and "Grand Rounds" to share learnings and best practices.

Strategic Collaboration and Capability Development:

• Foster collaboration with Epidemiologists, Medical Affairs, and Clinical Development Leaders to strengthen evidence generation plans
• Ensure support for implementing cross-cutting priorities such as Real-World Evidence, R&D Franchise optimization, and Digital Data Strategy.

Why You?

Working model
This role is hybrid. You will be based in Belgium, UK, USA or Itally with a mix of on-site collaboration and remote work. Expect regular on-site presence for team and cross-functional activities.

Basic Qualifications:

• Medical Doctor 
• 10+ years' experience in vaccines clinical development, including in late phase clinical trials of vaccines
• People Leadership experience, including ability to lead and inspire teams and allocate resources strategically
• Experience in working cooperatively with stakeholders in scientific, academic, regulatory and political communities
• Ability to produce scientific communications with clarity, accuracy and rigour
• Understanding of scientific, medical, regulatory and digital data environments, practices and requirements
• Understanding of local and global pharmaceutical industry, competitive landscape, how end-to-end life and revenue cycles operate
• Proven track record of effectively applying medical expertise to make good clinical decisions, in accordance with appropriate SOPs, policies, guidance and codes

Preferred Qualification

• Postgraduate clinical training, clinical residency or specialty training in Infectious Diseases, Paediatric, Internal Medicine or related field is desirable

What we value in you
You put patients at the centre of your work. You lead with humility and clarity. You make decisions based on evidence and practical judgement. You listen well and bring people together. You are committed to inclusion and to developing others.

How to apply
We welcome candidates with varied backgrounds and career paths. If you are excited by this role and want to help bring vaccines to patients, please apply. We look forward to hearing how your skills and ambitions match this opportunity.

• 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 $309,750 to $516,250. 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 167,250 to EUR 278,750Belgium Salary Range / Fourchette salariale Belgique: EUR 190,500 to EUR 317,500The 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 salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process. Please note salaries vary by country based on the candidate's skills, experience, education level and the market rate for the role. Offers are typically made within the advertised range based on the candidate's skills, experience and qualifications, with the upper end generally reserved for highly experienced candidates or other exceptional circumstances aligned with these criteria.

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 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.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - usrecruitment.adjustments@gsk.com

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

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