Medical Director – Clinical Development (Neurology)

Overview

• Drive clinical development programs in neurology, advancing innovative therapies to improve patient outcomes and contribute to medical science.
• Collaborate with multidisciplinary teams to design impactful strategies for neurological conditions and therapeutic advancements.
• Engage with regulatory authorities to ensure compliance and successful clinical program execution.
• Contribute to research expansion and foster innovation in neurology treatments and clinical strategies.
• Participate in strategic planning for neuroscience research and development initiatives.
• Hybrid work arrangement offering flexibility and relocation support for eligible candidates.
• Opportunity to engage with thought leaders and advocacy groups to enhance clinical initiatives and patient care.

Key Responsibilities & Duties

• Design and implement protocols for clinical trials, ensuring scientific rigor and compliance with industry standards.
• Provide medical oversight and monitoring for Phase 2 and Phase 3 trials, ensuring quality and efficacy.
• Author and review clinical protocols, regulatory documents, and scientific publications.
• Engage in strategic discussions on asset prioritization and clinical development plans.
• Represent the organization at clinical sites, advisory boards, and industry conferences.
• Manage operational aspects of clinical projects to meet performance benchmarks and timelines.
• Build and maintain relationships with investigators and thought leaders globally to enhance program impact.
• Contribute to regulatory interactions and submissions with critical insights and expertise.

Job Requirements

• Doctor of Medicine (MD) with specialization in Psychiatry or Neurology.
• Board Certification in Neurology or Psychiatry is highly preferred.
• Minimum of 2 years of pharmaceutical industry experience; 3 years preferred.
• Experience in early and late-stage clinical programs, with emphasis on late-stage trials.
• Proven ability to interact with global regulatory agencies and manage NDA/BLA submissions.
• Strong leadership and collaborative skills in matrixed environments.
• Excellent communication skills for engaging with senior management and external stakeholders.
• Self-driven with exceptional task prioritization and deadline management abilities.
• Detail-oriented expertise in reviewing medical and trial-related documentation.