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Vice President, Clinical Development-Neuroscience

Job in California, Moniteau County, Missouri, 65018, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-07-09
Job specializations:
  • Management
    Healthcare Management
Salary/Wage Range or Industry Benchmark: 200000 - 250000 USD Yearly USD 200000.00 250000.00 YEAR
Job Description & How to Apply Below
Location: California

Position:
Vice President, Clinical Development—Neuroscience Responsibilities

  • Lead the strategic direction and execution of neuroscience clinical development programs from early- to late-stage, ensuring scientific robustness and regulatory alignment.
  • Collaborate cross-functionally with discovery research, translational medicine, regulatory affairs, pharmacovigilance, biometrics, clinical pharmacology, medical affairs, and clinical operations to execute clinical development plans.
  • Drive preparation, submission, and management of regulatory filings (e.g., clinical trial applications, investigator brochures, study protocols, BLA/NDA, MAA) aligned with global guidelines (FDA, EMA).
  • Analyze, interpret, and communicate data to inform decisions and guide clinical development strategy.
  • Establish relationships with KOLs, clinical investigators, and external stakeholders to advance clinical initiatives.
  • Manage clinical trial budgets, timelines, and resources to deliver high-quality outcomes.
  • Present clinical progress, data outcomes, and recommendations to executive leadership and external partners.
  • Monitor industry trends, scientific advancements, and regulatory developments.
  • Identify clinical development risks in timelines, budgets, or regulatory pathways and develop contingency plans.
Required
  • MD or MD/PhD with board certification in Neurology/Neuroscience (or related field).
  • 15–20 years clinical development experience focused on CNS indications.
  • Proven leadership designing, managing, and executing Phase I–III trials.
  • Senior/executive-level experience leading clinical development teams (biotech/pharma).
  • In-depth knowledge of global regulatory requirements and clinical development processes (e.g., HA meetings, briefing books).
  • Strong leadership, strategic thinking, and communication; ability to influence across functions.
  • Ability to work in a fast-paced environment; manage multiple priorities.

    Preferred
    • Experience with regulatory submissions and clinical trial oversight in biotech/pharma.
    • Familiarity with emerging neurology trends and therapeutic modalities.
    Benefits
    • Flexible work schedules, remote opportunities, and work-life balance.
    • Shuttle service from BART, Cal Train, and the Ferry.
    • Competitive base salary plus equity participation; employee stock purchase plan.
    • Comprehensive health benefits: medical, dental, vision, 401(k), flexible spending plans, and other benefits.
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