Lead clinical development initiatives in neurology and advance innovative therapies. Collaborate with global experts and regulatory authorities to shape impactful strategies. Hybrid work model with relocation support for eligible candidates.
Medical Director – Clinical Development (Neurology)
in Healthcare + Life Sciences PermanentJob Detail
Job Description
Overview
- Lead clinical development initiatives in neurology, driving innovative therapies and advancing patient care.
- Collaborate with multidisciplinary teams to shape impactful clinical strategies and programs.
- Engage with global regulatory authorities to ensure compliance and successful program execution.
- Contribute to strategic planning for therapeutic advancements in neuroscience.
- Participate in expanding research efforts and fostering innovation in neurology.
- Hybrid work arrangement with relocation support for eligible candidates.
- Opportunity to work on diverse clinical programs across development stages.
- Collaborate with thought leaders and advocacy groups to enhance clinical initiatives.
Key Responsibilities & Duties
- Design and implement protocols for early- and late-stage clinical trials in neurology.
- Serve as Global Clinical Lead, overseeing clinical subteams for multiple programs.
- Provide medical oversight and monitoring for Phase 2 and Phase 3 trials.
- Author and review 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.
- Build and maintain relationships with investigators and thought leaders globally.
- Contribute to regulatory interactions and submissions with critical insights.
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.
- 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.
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