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Global drug and device development services

Medical Director (Psychiatry)

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

About the Job

Requirements

  • An MD and residency training in Psychiatry are required.
  • Extensive drug development experience in psychiatry, including Phase I–III clinical development in schizophrenia, bipolar disorder, ADHD, and major depressive disorder, is required.
  • Five or more years of experience in the pharmaceutical industry in a Clinical Development role as a Medical Director is required.
  • Experience interacting with and presenting to senior management and external audiences is required.
  • The ability to manage complexity and ambiguity in a highly matrixed work environment is required.
  • Strong leadership and collaborative interpersonal skills are required.
  • The ability to work independently, prioritize tasks effectively, and meet expected timelines is required.
  • The ability to perform thorough reviews of medical and clinical trial-related documents in a timely manner is required.
  • The legal right to work in the country where the role is based is required.

Responsibilities

  • Serve as the Global Clinical Lead and Medical Monitor for one or more studies, including participation on the clinical sub-teams of those programs.
  • Contribute directly to authoring protocols, clinical study reports, study documents, regulatory documents, and external publications.
  • Provide medical review of clinical trial data and medical monitoring of clinical trials.
  • Interact with senior management regarding data presentations, trial updates, and discussions of executional and strategic development issues.
  • Contribute to strategic discussions related to clinical development plans and indication prioritization.
  • In collaboration with Clinical Operations, oversee and coordinate the operational aspects of ongoing projects to ensure time, cost, and quality objectives are met.
  • Ensure Clinical Development Standard Operating Procedures facilitate effective clinical research programs and comply with clinical, medical, and industry standards.
  • Review and contribute to regulatory documents and regulatory interactions as needed.

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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