Medical Director - 2026 Global Talent Program

About the Company

We are seeking a highly experienced and motivated Medical (Associate) Director to lead and oversee clinical development programs in the field of non-oncology. The ideal candidate will have a strong background in clinical research, a deep understanding of immunology disease, and a proven track record of successfully advancing clinical trials from Phase I through Phase IV. This role requires strategic leadership, scientific expertise, and the ability to collaborate cross-functionally to drive the development of innovative therapies.

About the Role

Essential Job Functions:

Global Clinical Development Strategy:

• Lead the design, planning, and execution of clinical trials for non-oncology therapeutic area, ensuring alignment with regulatory requirements and company objectives.
• Provide medical and scientific expertise to guide the development of clinical protocols, study designs, and regulatory submissions.
• Leading the medical content creation for EMA and US FDA interactions and submissions.

Global Clinical Trial Oversight:

• Serve as the medical monitor for global clinical trials, ensuring patient safety, data integrity, and compliance with GCP and regulatory standards.
• Review and interpret clinical data, identify trends, and provide medical input for decision-making.

Cross-Functional Collaboration:

• Work closely with biostatistics, regulatory affairs, pharmacovigilance, and other teams in other countries or territories to ensure seamless execution of clinical programs.
• Collaborate with external stakeholders, including investigators, key opinion leaders (KOLs), and regulatory agencies in EU, US and other countries.

Scientific Leadership:

• Stay abreast of advancements in non-oncology research and contribute to the scientific direction of the company.
• Represent the company at scientific conferences, advisory boards, and regulatory meetings.

Qualifications

• Medical Degree (MD or equivalent) with preferred qualification in immunology-related field (e.g. rheumatology, diabetes, SLE).
• Minimum of 2 - 5 years of industry experience in clinical research.
• Proven track record of leading clinical trials and contributing to regulatory submissions (e.g., IND, NDA, BLA).
• Proven success record in Phase I-III clinical research studies, trial design, IND submission, and marketing approval-directed filings.
• Experience communicating and interacting with investigators, KOLs, and advisors.
• Hands on experience with Scientific Advice, Paediatric Investigational Plans and Marketing Authorizations process of European Medical Agency (FDA preferred too).
• Experience working with the principles and techniques of data analysis, interpretation and clinical relevance.
• Proven ability to “build a case,” both with internal scientific management and the Company’s partners / collaborators.
• Ability to work in a fast-paced, dynamic environment and manage multiple priorities.
• Experience with biologics, small molecules, or novel therapeutic modalities in non-oncology diseases.
• Familiarity with global regulatory requirements and guidelines.