Director of Regulatory Affairs at Enigma Search in South San Francisco, California

Posted in Other 8 days ago.

Type: full-time





Job Description:

Are you a seasoned Regulatory Affairs professional ready to make a significant impact on human health? We are seeking a strategic and driven Director of Regulatory Affairs to join a pioneering research and development company focused on extending healthy lifespan.

This is an exceptional opportunity to play a pivotal role in developing and implementing innovative regulatory strategies for groundbreaking programs. You will collaborate with cross-functional teams and external partners, driving regulatory success from IND-enabling studies through clinical proof-of-concept and beyond.

Your Impact:
  • Develop and execute global regulatory strategies for assigned programs, including first-in-class therapies and programs with external partnerships.
  • Lead interactions with global health authorities, preparing briefing packages and ensuring clear communication.
  • Collaborate with executive leadership to define regulatory strategies aligned with the company's mission.
  • Oversee the preparation and submission of regulatory applications, ensuring accuracy and timeliness.
  • Develop effective CMC regulatory strategies in collaboration with Technical Operations.
  • Provide strategic regulatory input to development teams, protocols, reports, and other critical documents.
  • Stay ahead of global regulatory changes, communicating updates and developing proactive strategies.
  • Collaborate with cross-functional teams and external consultants.

What You Bring:
  • Master's degree in a life science discipline (PhD preferred).
  • Minimum of 10 years of regulatory affairs experience in industry, academia, or clinical research, with experience in rare disease development and/or novel endpoints.
  • Proven track record of developing regulatory submissions, including experience with major approvals (NDA, BLA, MAA, etc.).
  • Strong knowledge of global regulations (FDA, EMA, etc.).
  • Experience with mechanisms to expedite agency interactions.
  • Advanced skills in creating and assessing regulatory proposals and leading health authority interactions.
  • Excellent communication and influencing skills.
  • Self-motivated, strategic thinker with strong problem-solving skills.
  • Exceptional organizational and prioritization skills.
  • Ability to thrive in a fast-paced, collaborative, start-up environment.
  • Must be willing to work onsite at least four days per week.

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