Director of Regulatory Affairs
Enigma Search
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 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. ($275,000-$280,000 base with 25% annual bonus AND $125,000 annual CASH bonus) #J-18808-Ljbffr Enigma Search
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Denali Therapeutics Inc in South San Francisco seeks a Regulatory Affairs professional to develop and implement regulatory strategies for complex programs. The ideal candidate has over 10 years of experience, including 8 years in regulatory affairs, and excels in communication...$245k - $302k
Initial Therapeutics, Inc. is seeking a Senior Director of Medical Writing in South San Francisco. The ideal candidate will provide leadership on regulatory documents and oversee a team, requiring an extensive background in oncology and successful IND submissions. Competitive...- Initial Therapeutics, Inc. is seeking an Associate Director, Quality Management Systems (QMS) in South San Francisco. This role involves... ..., implementing quality policies, and ensuring compliance with regulatory standards in the development of new cancer therapies. The...
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Structure Therapeutics Inc. is seeking a Senior Director of GMP Quality Assurance in South San Francisco. This role leads the global GMP QA strategy, ensuring compliance and quality system design as the company advances from clinical to commercial stages. Qualified candidates...$235k - $285k
About the Role Septerna is seeking an experienced and highly motivated Director/Senior Director of Regulatory Affairs to lead regulatory strategy and execution across our discovery and development programs. This individual will be responsible for developing and implementing...Full time$140k - $214k
...Summary Vera is seeking a Senior Manager, Regulatory CMC to join an experienced, fast‑paced... ...Senior Manager will report to the Senior Director of Regulatory CMC and will be... ...regional requirements. Represent Regulatory Affairs on cross‑functional project teams. Evaluate...Flexible hours- Position Summary Responsible for leading regulatory review of advertising, promotional, and other external communications to ensure compliance... .... Targeting 10 years progressively responsible Regulatory Affairs experience focused on advertising/promotional regulations (or...
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