Interventional Study Scientist Director

Locations: GSK HQ, New Oxford Street & USA - Upper Providence

Reports to: Head of Interventional & Supported Studies

Join GSK's Medical Affairs team and be part of a global organization that drives innovation, scientific excellence, and patient-centered solutions. As a member of the Medical Affairs organization, you'll collaborate with cross-functional teams to shape clinical practice, engage with healthcare professionals, and deliver on our promise to help people do more, feel better, and live longer.

This role offers an exciting opportunity to lead the scientific design and execution of interventional clinical studies within the Medical Affairs organization for oncology or hematology assets. You will shape data generation strategies, ensure studies are conducted with the highest standards of quality and ethics, and collaborate with cross-functional teams to deliver impactful results.

In this role, you will:

• Design and oversee interventional clinical studies, ensuring alignment with strategic objectives and evidence plans.
• Provide scientific oversight for study protocols, analysis plans, and interpretation of study data.
• Ensure patient safety and scientific integrity throughout study conduct, including medical governance and monitoring.
• Collaborate with cross-functional teams to ensure seamless execution and delivery of clinical programs.
• Prepare and present study results for scientific meetings, publications, and regulatory submissions.
• Engage with internal and external stakeholders, including investigators and thought leaders, to enhance study design and execution.

• Advanced degree in a relevant scientific discipline (MD, PhD, PharmD, or equivalent).
• Specialized experience in oncology, pulmonology, hepatology or a related therapeutic area.
• Considerable experience in clinical research, including interventional studies.
• Proven experience designing and executing clinical trials with demonstrated impact.
• Strong understanding of regulatory requirements and industry best practices for clinical research.
• Experience leading cross-functional teams in a matrixed environment.
• Excellent communication and organizational skills.

• Experience leading multi-country or global interventional studies.
• Experience collaborating with regulatory authorities.
• Familiarity with innovative approaches in clinical trial design and execution.
• Exposure to working with key opinion leaders, investigators, and external partners.
• Experience developing scientific content for publications and regulatory submissions.
• Understanding of digital tools and methodologies for evidence generation.

You will join a team focused on scientific rigour and patient impact. You will gain leadership exposure across functions and grow your clinical development expertise. We value inclusion, work-life balance, and career development. We offer a flexible working culture.

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.