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Risk Consulting - Enterprise Risk - Sr Manager - Life Sciences - Regulatory Affairs

LinkedIn EY Hartford, CT
Mid-Senior level Posted April 3, 2026 3 variants Job link
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Requirements
  • Proven experience in regulatory compliance within the life sciences sector, with a focus on regulatory submissions.
  • Strong understanding of the FDA regulatory process and the associated risks and challenges.
  • 8+ years of Regulatory Affairs experience with a strong focus on regulatory submissions in the life sciences industry.
  • Demonstrated experience leading major global submissions (FDA and at least one other major health authority).
  • Strong working knowledge of applicable regulations (e.g., 21 CFR, ICH guidelines, EU regulations).
  • Experience with global regulatory strategies and lifecycle management.
  • Strong project management and risk management capabilities.
  • Prior experience supporting inspections, health authority interactions, or regulatory inquiries.
  • Ability to contribute to go-to-market strategies, thought leadership, or practice development initiatives.
  • Ability to travel domestically and internationally.
Preferred Skills
  • Proven experience managing teams and complex, cross-functional initiatives.
  • Excellent written and verbal communication skills, with the ability to engage senior stakeholders.
  • Experience working in a consulting, CRO, or matrixed corporate environment preferred.
  • Ability to travel domestically and internationally.
  • Travel expectation up to 40%.
  • We are interested in passionate leaders with strong delivery capability, and a strong desire to stay on top of trends in the life sciences industry.
Education
  • (Not required) – A bachelor’s or master’s degree in in Life Sciences, Pharmacy, Regulatory Affairs, or a related field or a related field (advanced degree preferred)
  • (Not required) – Ideally, you’ll also have