Join our team as a Medical Director and lead impactful clinical development initiatives. Collaborate with global experts to advance neurology therapies. Experience a hybrid work model with relocation support.

Medical Director – Clinical Development (Neurology)
in Healthcare + Life Sciences PermanentJob Detail
Job Description
Overview
- Lead clinical development efforts in neurology and neuropsychiatric indications, contributing to groundbreaking therapies.
- Collaborate across departments and levels within the organization to drive impactful projects.
- Engage with global regulatory authorities and industry leaders to shape clinical strategies.
- Participate in strategic planning for therapeutic priorities and modalities in neuroscience.
- Contribute to the expansion of research and development efforts in neurology.
- Hybrid work arrangement with relocation support for qualified candidates.
- Opportunity to work on both early and late-stage clinical programs.
- Collaborate with thought leaders and patient advocacy groups to advance clinical initiatives.
Key Responsibilities & Duties
- Design and execute protocols for early- and late-stage clinical trials in neurology.
- Serve as Global Clinical Lead, managing clinical subteams for multiple programs.
- Provide medical oversight and monitoring for Phase 2 and Phase 3 trials.
- Contribute to authorship of protocols, regulatory documents, and external publications.
- Engage in strategic discussions regarding asset prioritization and clinical development plans.
- Represent the organization at clinical sites, advisory boards, and major conferences.
- Oversee operational aspects of projects to meet performance expectations.
- Develop collaborative relationships with investigators and thought leaders globally.
- Critically review and contribute to regulatory interactions and submissions.
Job Requirements
- Doctor of Medicine (MD) with specialization in Psychiatry or Neurology.
- Board Certification in Neurology or Psychiatry preferred.
- Minimum of 2 years of pharmaceutical industry experience; 3 years preferred.
- Experience in early and late-stage clinical programs, with a preference for late-stage.
- Proven ability to interact with global regulatory agencies and manage NDA/BLA submissions.
- Strong leadership and collaborative skills in matrixed environments.
- Outstanding communication skills for engaging with senior management and external audiences.
- Self-motivated with excellent task prioritization and deadline management abilities.
- Detail-oriented expertise in reviewing medical and trial-related documents.
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