Interventional Study Scientist Medical Director

Reports to: Head of Interventional & Supported Studies

In this role, you will:
- 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.

Basic Qualifications & Skills (required):
- 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.

Preferred Qualifications & 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.

Application instructions:
- Use the ‘cover letter’ or your CV to describe how you meet the competencies for the role.