Global Development Medical Director, Late Respiratory and Immunology Clinical Development

Overview

In this role you guide medical and scientific leadership for global late-stage development of respiratory and immunology medicines. You influence trial design, interpretation, and medical input for regulatory and labeling matters, collaborating with cross-functional teams and external experts. You drive medical monitoring and contribute to publications, regulatory documents, and strategic development plans to demonstrate value and safety. This is a global, fast-paced position offering close interaction with regulators, clinicians, and scientists to shape life-changing medicines.

Pay / Benefits

• hybrid/in-office work with minimum three days per week in the office
• flexible working arrangements
• inclusive and equitable environment
• reasonable adjustments/accommodations on request
• collaborative, global team culture

Responsibilities

• Provide medical and scientific leadership across global late-stage development programs (Ph2b and beyond) in respiratory and immunology.
• Lead design, execution, and interpretation of pivotal clinical trials and studies assessing risk/benefit and value.
• Build and maintain relationships with external scientific experts and key stakeholders.
• Collaborate with Patient Safety, Regulatory Affairs, and Clinical Operations to ensure integrated development.
• Lead medical monitoring of trials and contribute to regulatory documents and interactions with authorities.
• Develop and review protocols, informed consent, and investigator’s brochure; support scientific publications and conference presentations.

Key requirements

• MD or MD/PhD degree
• 3+ years of pharmaceutical industry experience
• 3+ years of clinical research experience in academic or clinical practice
• Demonstrated partnership and cross-country collaboration skills
• Fluent in English (oral and written) with strong presentation and communication abilities

• partnership and collaboration
• leadership across cultures
• effective communication
• medical leadership in drug development
• clinical trial design, execution, and interpretation
• medical monitoring of trials

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