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Interventional Study Scientist Medical Director

Job in Waltham, Middlesex County, Massachusetts, 02254, USA
Listing for: GSK
Full Time position
Listed on 2026-09-12
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 187275 - 312125 USD Yearly USD 187275.00 312125.00 YEAR
Job Description & How to Apply Below

Locations – GSK HQ UK, New Oxford Street & USA - Upper Providence/ Waltham MA

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. 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. 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:

  • Design and oversee interventional clinical studies, ensuring alignment with strategic objectives and evidence plans.
  • Facilitate medical governance, review safety data and guide risk mitigation actions.
  • 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.
Basic

Qualifications & Skills
  • Advanced degree in a relevant scientific discipline (MD, PhD, PharmD, or equivalent).
  • Substantial experience leading interventional clinical studies in a therapeutic area such as oncology/haematology/ Immunology, Specialty, and other GSK-related therapeutic areas of interest.
  • 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.
  • Excellent communication and organizational skills.
Preferred Qualifications & Skills
  • Experience leading global Phase IIIb/IV 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.
  • Experience leading cross-functional teams in a matrixed environment.
Why You?

We are seeking candidates who want to grow into a visible scientific leader. This is a hybrid role based in either United Kingdom or United States with an expected in-office presence of around two to three days per week. You will have the opportunity to shape strategy, mentor colleagues, and influence clinical evidence generation across teams.

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