Medical Director

Overview

• Lead medical strategy and clinical development for innovative treatments, advancing healthcare solutions in respiratory and inflammatory conditions.
• Serve as the primary medical authority, guiding scientific and clinical inquiries across interdisciplinary teams.
• Provide strategic leadership for clinical trials, including protocol development and comprehensive study oversight.
• Collaborate with senior leadership to align clinical strategies with organizational goals and objectives.
• Engage with key opinion leaders and stakeholders to foster collaboration and advance clinical programs.
• Contribute to the development and prioritization of product pipelines and clinical indications.
• Support investor relations through impactful presentations and participation in strategic meetings.
• Ensure compliance with regulatory standards and best practices in clinical development processes.

Key Responsibilities & Duties

• Supervise medical and safety conduct of clinical studies, ensuring data integrity and publication readiness.
• Develop and amend clinical trial protocols and study-related documents in collaboration with leadership teams.
• Lead product profile pipeline development and prioritize clinical indications based on strategic goals.
• Train study staff on protocol implementation and ensure adherence to study guidelines and standards.
• Support site and investigator selection for clinical trials, fostering effective partnerships.
• Act as Medical Monitor, overseeing study data and addressing inquiries from stakeholders.
• Build and maintain relationships with key opinion leaders, developing product champions within the medical community.
• Provide updates to the Board of Directors and investors, participating in strategic decision-making meetings.
• Lead post-market introduction of products into standard medical practices, ensuring successful adoption.

Job Requirements

• Doctor of Medicine (MD) with proven experience in clinical trial and medical leadership roles.
• Background in respiratory medicine or NICU, with expertise in drug development processes.
• Proficiency in collaborating with Contract Research Organizations (CROs) and managing clinical partnerships.
• Strong communication skills and fluency in English for effective stakeholder engagement.
• Experience in protocol development, study oversight, and data analysis for clinical trials.
• Ability to establish and nurture relationships with key opinion leaders and stakeholders.
• Familiarity with regulatory standards and compliance in clinical development processes.
• Capability to lead post-market product introduction into medical practices effectively.
• Minimum of 1 year of relevant experience, with 3 years preferred for optimal expertise.