Interventional Study Scientist Director

GSK

1d

About The Position

Join GSK's Medical Affairs team and be part of a global organization that drives innovation, scientific excellence, and patient-centered solutions. At GSK, we are committed to improving lives by ensuring the safe and effective use of our medicines and vaccines, bridging critical scientific insights with impactful healthcare strategies. As a member of Medical Affairs organisation, 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 assets. You will play a pivotal role in shaping data generation strategies, ensuring studies are conducted with the highest standards of quality and ethics, and collaborating with cross-functional teams to deliver impactful results. We are looking for a leader who is passionate about advancing science, thrives in a collaborative environment, and is motivated to make a meaningful impact on patient outcomes.
In this role, you will:
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

Requirements

• Advanced degree in a relevant scientific discipline (MD, PhD, PharmD, or equivalent).
• 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.

Nice To Haves

• Specialized experience in oncology, pulmonology, hepatology or a related therapeutic area.
• 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.

Responsibilities

• 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.

Benefits

• 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.
• If you are ready to make a tangible difference and grow with us, please apply.
• We are committed to creating an inclusive workplace where everyone can thrive.
• If you are passionate about making a difference and have the skills and experience, we are looking for, we encourage you to apply.

What This Job Offers

• Job Type: Full-time
• Career Level: Director
• Education Level: Ph.D. or professional degree