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Global drug and device development services

Vice President, Drug Development Services (CNS/Psychiatry)

Biology & BiotechConfirmed live in the last 24 hours
Full-time

About the Job

Requirements

  • An MD with specialization in Neurology, Psychiatry, or a closely related central nervous system discipline is required.
  • At least 10 years of progressive leadership experience in drug development, with significant expertise in central nervous system and psychiatric therapeutic areas across pharmaceutical, biotechnology, or contract research organization environments is required.
  • Demonstrated success advancing assets through multiple stages of development, including clinical, regulatory, and strategic decision-making that supports successful development milestones is required.
  • Deep understanding of global regulatory requirements and experience guiding development strategies across major regulatory agencies is required.
  • Proven ability to influence and build credibility with executive leadership, including chief executive officers, chief medical officers, therapeutic area heads, and other senior stakeholders is required.
  • Strong experience leading multidisciplinary global teams, including talent development, organizational leadership, budget accountability, and resource management is required.
  • A successful track record supporting business growth, client engagements, and complex drug development partnerships is required.
  • An extensive professional network within pharmaceutical, biotechnology, academic, and regulatory communities is required.
  • Must live in the United States, United Kingdom, or Ireland and be able to travel up to 25%.
  • Must have the legal right to work in the country where the role is based.

Responsibilities

  • Provide strategic scientific and medical leadership for central nervous system and psychiatry development programs spanning Phase I through late-stage clinical development, ensuring robust clinical, regulatory, and commercial strategies.
  • Serve as a trusted advisor to senior client stakeholders, delivering consulting engagements and guiding decisions related to protocol design, development planning, patient selection, endpoints, and overall program strategy.
  • Lead multidisciplinary Drug Development Services teams, fostering a high-performance culture focused on collaboration, innovation, scientific excellence, and client success.
  • Drive the design and execution of integrated drug development solutions, including clinical development strategies, feasibility assessments, regulatory planning, risk mitigation, and program optimization.
  • Build and maintain relationships with investigators, key opinion leaders, advisory boards, regulatory agencies, and industry stakeholders to advance client objectives and strengthen ICON's market presence.
  • Partner with Business Development teams to support strategic growth initiatives, including proposal development, client presentations, bid defenses, and scientific leadership during business development activities.
  • Represent ICON as an industry thought leader through participation in scientific conferences, professional organizations, client forums, and external speaking engagements.

About the Company

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Global drug and device development services

This company provides consulting, development, and commercialization support for drugs and medical devices through a global network of offices. Its team across 53 countries offers end-to-end services, from strategy and regulatory work to manufacturing and market access, helping clients shorten development time, lower costs, and raise quality. It differentiates itself with wide geographic reach and a clear focus on reducing time to market and cost while leveraging deep experience across many therapeutic areas. Its goal is to help clients accelerate the development of life-saving products and improve quality of life by delivering reliable information, practical solutions, and solid performance.

Company size
10,001+
Company stage
IPO
Headquarters
Ireland
Founded
1990

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