Medical Director – Clinical Development – Neurology

Medical Director – Clinical Development – Neurology Overview

• The Medical Director will lead clinical development initiatives in neurology and neuropsychiatric indications, including sleep disorders.
• Collaborate cross-functionally to ensure projects align with organizational goals and regulatory standards.
• Engage with global regulatory authorities, scientific organizations, and key thought leaders to advance therapeutic priorities.
• Contribute to strategic discussions on clinical development plans and indication prioritization.
• Participate in protocol design, medical review of clinical trial data, and generation of clinical study reports.
• Represent the client at external events, including advisory boards, investigator meetings, and medical conferences.
• Mentor junior clinical research colleagues and contribute to business development activities as required.
• Work in a hybrid environment, balancing office presence with remote flexibility.

Medical Director – Clinical Development – Neurology Key Responsibilities & Duties

• Design and execute protocols for clinical research trials in neurologic disorders.
• Serve as the Global Clinical Lead for programs, leading clinical subteams effectively.
• Contribute to authorship of protocols, clinical study reports, and regulatory documents.
• Provide medical review and monitoring for Phase 2 and Phase 3 clinical trials.
• Engage with senior management and participate in project teams.
• Develop collaborative relationships with investigators and thought leaders globally.
• Ensure compliance with clinical/medical standards and industry regulations.
• Oversee operational aspects of projects to meet time, cost, and quality expectations.
• Critically review and contribute to regulatory interactions, including INDs and NDAs.

Medical Director – Clinical Development – Neurology Job Requirements

• Doctor of Medicine (MD) with board certification in Neurology.
• Minimum of two years of pharmaceutical industry experience, with expertise in drug development.
• Proven experience interacting with global regulatory agencies and successful NDA/BLA submissions.
• Strong written and verbal communication skills, with ability to present to senior management.
• Ability to manage complexity and ambiguity in a matrixed work environment.
• Leadership and collaborative interpersonal skills, with mentoring capabilities.
• Proficiency in reviewing medical and trial-related documents thoroughly and timely.
• Flexibility to work in a hybrid model, balancing office and remote presence.