Executive Director Global Regulatory Affairs Job at EPM Scientific, Newark, NJ

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  • EPM Scientific
  • Newark, NJ

Job Description

A leading global biopharmaceutical organization is seeking a seasoned Executive Director of Global Regulatory Strategy to lead regulatory initiatives across a diverse portfolio of innovative therapies. This is a high-impact, hands-on leadership role ideal for a strategic thinker with deep regulatory expertise and a passion for advancing global health. This is a highly visible senior leadership position that will involve regular interactions with senior executive of the organization while overseeing the RA strategy from pre-clinical through marketing, on a global scale.

Responsibilities:

  • Provide strategic regulatory leadership for global development programs and marketed products across designated therapeutic areas.
  • Lead and mentor a team of regulatory professionals in the development and execution of global regulatory strategies.
  • Serve as the senior regulatory representative on cross-functional project teams throughout the product lifecycle.
  • Advise executive leadership on U.S. and international regulatory matters, ensuring alignment with evolving global standards.
  • Oversee planning and execution of regulatory agency interactions, including meetings with major health authorities (e.g., FDA, EMA, PMDA).
  • Actively participate in Health Authority GCP inspections (e.g., FDA, EMA, PMDA) including responding to observations and development of corrective actions.
  • Support regulatory inspections and audits, including response development and implementation of corrective actions.
  • Monitor and interpret global regulatory trends, providing strategic insights and direction on emergency policy & regulatory intelligence.
  • Drive continuous improvement in regulatory processes and team performance.
  • Manage timelines, budgets, and resource planning for regulatory programs.
  • Contribute to global regulatory policy initiatives and cross-functional governance committees.

Qualifications

  • Bachelor's degree in a scientific discipline required; advanced degree (MS, PharmD, PhD, or equivalent) preferred.
  • Minimum of 20 years of industry experience, including at least 15 years in regulatory affairs within the biopharma sector.
  • Proven leadership experience managing regulatory teams and complex global submissions.
  • Demonstrated success in leading regulatory strategy for major marketing applications (e.g., NDA, BLA, MAA).
  • Strong track record of engagement with global regulatory agencies (FDA, EMA) and successful negotiation of regulatory pathways.
  • Experience in managing the preparation of a marketing application (NDA/BLA/MAA) in CTD format for a major market (US, EU, Canada).
  • Strategic mindset with the ability to navigate ambiguity and make informed decisions.
  • Excellent communication and presentation skills, with the ability to influence at all levels of the organization.

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