Medical Director

Overview

• Lead medical strategy and direction for clinical development programs focused on respiratory and inflammatory diseases.
• Act as the primary medical resource for scientific and clinical inquiries within the organization.
• Provide medical leadership for clinical trials, including protocol development and study oversight.
• Collaborate with senior leadership to align clinical strategies with organizational goals.
• Engage with key opinion leaders and stakeholders to advance clinical programs.
• Contribute to the development and prioritization of product pipelines and clinical indications.
• Support investor relations through participation in meetings and preparation of materials.
• Ensure compliance with regulatory standards and best practices in clinical development.

Key Responsibilities & Duties

• Supervise medical and safety conduct of clinical studies, including data analysis and publication preparation.
• Develop and amend clinical trial protocols and study-related documents in collaboration with leadership.
• Lead product profile pipeline development and prioritize clinical indications.
• Train study staff on protocol implementation and ensure adherence to study guidelines.
• Support site and investigator selection for clinical trials.
• Act as Medical Monitor, overseeing study data and addressing inquiries from stakeholders.
• Build and maintain relationships with key opinion leaders and develop product champions.
• Provide updates to the Board of Directors and investors, participating in strategic meetings.
• Lead post-market introduction of products into standard medical practices.

Job Requirements

• Doctor of Medicine (MD) with clinical trial and medical leadership experience.
• Background in respiratory medicine or NICU, with drug development expertise.
• Proficiency in working with Contract Research Organizations (CROs).
• Strong communication skills and fluency in English.
• Experience in protocol development, study oversight, and data analysis.
• Ability to build relationships with key opinion leaders and stakeholders.
• Familiarity with regulatory standards and compliance in clinical development.
• Capability to lead post-market product introduction into medical practices.
• Minimum of 1 year of experience, with 3 years preferred.