Interventional Study Scientist Medical Director

Reports to:

Head of Interventional & Supported Studies

• 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.
• Prepare and present study results for scientific meetings, publications, and regulatory submissions.
• Engage internal/external stakeholders (e.g., investigators and thought leaders) to enhance study design and execution.

• Advanced degree in a relevant scientific discipline (MD, PhD, PharmD, or equivalent).
• Substantial experience leading interventional clinical studies in therapeutic areas such as oncology/haematology/immunology/specialty.
• 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.
• Excellent communication and organizational skills.

• Experience leading global Phase IIIb/IV interventional studies.
• Experience collaborating with regulatory authorities.
• Familiarity with innovative clinical trial design/execution approaches.
• Experience developing scientific content for publications and regulatory submissions.
• Understanding of digital tools/methodologies for evidence generation.
• Experience leading cross-functional teams in a matrixed environment.