Director of Regulatory Affairs Job at Enigma Search, South San Francisco, CA

czM1YTdDbHNEejlaTG8vWW83ODY5VjZ6aWc9PQ==
  • Enigma Search
  • South San Francisco, CA

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.

Job Tags

Similar Jobs

ARAMARK

Food Service Director - Lead Dining Operations (San Francisco) Job at ARAMARK

 ...A leading food and facilities management company is seeking a Food Service Director in San Francisco, CA. This management role involves developing and executing dining solutions, overseeing operations, and building client relationships. Candidates should have a bachelors... 

SP Software Solutions

Scrum Master (Philadelphia) Job at SP Software Solutions

 ...Job Title: Scrum Master Location: Philadelphia, PA (Hybrid Onsite 3 Days/Week) Duration: 6+ Month Contract Job Description We are seeking an experienced Scrum Master to join our healthcare clients technology team in Philadelphia, PA. The ideal candidate will... 

Reyes Coca-Cola Bottling

CDL-A Drivers - Home Daily - Earn Up to $75k/Year + $3k Sign-On Bonus Job at Reyes Coca-Cola Bottling

 ...Job Description Reyes Coca-Cola Bottling is Now Hiring Local CDL-A Drivers in Kincheloe, MI!\nHome Daily - Earn Up to $75,000 Annually + Weekends Off!\n$3,000 Sign-On Bonus + Full Benefits Package \n\n Benefits:\n\n \n\t ~ Earn up to $75,000 annually \n\...