Associate Director Regulatory Affairs
$215.54k - $260.82kDenali Therapeutics
Associate Director, Clinical Regulatory page is loaded## Associate Director, Clinical Regulatorylocations: South San Franciscotime type: Full timeposted on: Posted 4 Days Agojob requisition id: R-1479Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients.We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients.The Associate Director, Clinical Regulatory is a highly motivated and creative individual with deep and broad regulatory experience and expertise. This individual is a Global Regulatory Leader accountable for the strategic and technical regulatory leadership of one or more development programs in neurodegenerative diseases. This leader is accountable for leading and overseeing global Health Authority interactions, project team support, regulatory intelligence activities, and proposing and implementing department initiatives in our drive to defeat neurodegeneration.**Key Accountabilities/Core Job Responsibilities**:***** Accountable for developing regulatory strategy for complex development programs; leads project teams in implementing and delivering the regulatory strategy across multiple programs/indications and/or programs of increasing complexity* Responsible for identifying regulatory risk and mitigation in support of development plans* Accountable for overseeing and directly leading global Health Authority interactions* Independently executes preparation, submission, and maintenance of regulatory applications, including initial applications, routine amendments, annual reports, IND safety reports, and correspondence with global Health Authorities* Participates in cross-functional teams, providing regulatory feedback and support* Partners with external vendors in support of regulatory document preparation and submission* Maintains up-to-date knowledge of the regulatory landscape, regulations, and guidelines* Identifies and maintains leadership/ownership of non-project activities* Complies with relevant governing laws, regulations, guidelines, and Denali SOPs* Develops, manages, and mentors junior regulatory professionals and contributes to creating a culture regulatory innovation and excellence; leads direct report(s), if applicable, through annual goal setting, growth planning, adherence to company policies, maintains training compliance and provides ongoing feedback on growth, development and areas of improvement.**Qualifications/Skills:*** Bachelor’s degree required. Advanced degree in life sciences strongly preferred.* 7+ years of relevant work experience required, including 6+ years in regulatory affairs* Thorough understanding of drug development process and the pharmaceutical industry and healthcare environment including regulatory requirements and policy trends* Strong experience with INDs/CTAs, NDAs/BLAs/MAAs, lifecycle management, interactions with Health Authorities, developing and implementing regulatory strategies with a proven track record of significant regulatory accomplishments.* Broad strategic skill set, including creativity and effectiveness in identifying and addressing major strategic challenges (e.g., competitive landscape, challenging therapeutic areas).* Skilled in influencing, partnership, and collaboration, including demonstrated ability to deliver on goals within a cross-functional team/partnership environment with a high level of professionalism* Excellent written and verbal communication and collaboration skills* Strong ability to prioritize workload and delegate appropriately* Well-prepared, competent, and confident when interacting with senior management,health authorities, and internal and external partners* Able to prospectively identify potential problems and to partner effectively and positively to solve issuesSalary Range: $215,544.00 to $260,822.00 . Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. Learn more at compensation and benefits information is based on Denali’s good faith estimate as of the date of publication and may be modified in the future.This compensation and benefits information is based on Denali’s good faith estimate as of the date of publication and may be modified in the future.Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class.“Life at Denali” is a living reflection of our values: trust, unity, grit and growth. These are not just words we share—they shape how we show up, collaborate and push boundaries together. From the lab to the community, across functions and milestones, our culture thrives on shared purpose and relentless pursuit. #J-18808-Ljbffr
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The Associate Director, IT Compliance is responsible for organising, leading and continuously improving Novotech’s IT Compliance function across... ..., ISO/IEC 27001:2022 certification activities, and regulatory compliance guidance for GxP computerised systems. This role...Contract workWorldwideFlexible hours$265k - $285k
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...medical breakthroughs. Position Description: Calico is seeking a Regulatory Director that will be responsible for, in collaboration with... ...develop effective CMC regulatory strategies Represent Regulatory Affairs on development teams and support development teams in...Full time$170k - $230k
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...goal of delivering meaningful therapeutics to patients. Associate Director, Clinical Regulatory The Associate Director, Clinical Regulatory is a highly... ...experience required, including 6+ years in regulatory affairs. Thorough understanding of drug development process and...Work experience placementLocal area- ...About the job Director, Regulatory Affairs 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...
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...and our mission's urgency. This role can be based out of either our Seattle, WA or South San Francisco, CA offices. The Director of Regulatory Affairs/Global Regulatory Lead (GRL) will be focusing on the development of cutting‑edge CAR‑T cell therapies in oncology. As...Temporary workLocal area- Position Title: Director, Regulatory Affairs (Strategy, Immunology and Inflammation) Nurix Therapeutics is a clinical stage biopharmaceutical... ...indications and identify potential risks and mitigation strategies associated with proposed strategies Work in close collaboration with...For contractorsWork at office
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...Director, Regulatory AffairsSkip to main content# CareersDirector, Regulatory Affairs page is loaded## Director, Regulatory AffairsApplylocations: South San Francisco, Californiatime type: Full timeposted on: Posted 29 Days Agojob requisition id: R468Cytokinetics is a...For contractors$171k - $223k
...drives the operational backbone of Denali's regulatory strategy, ensuring that every drug... ...actionable plans. The role shapes how Regulatory Affairs plans and resources its work,... ...Regulatory Program Managers and Program Directors to align regulatory timelines with corporate...Local areaShift work$180k - $210.5k
...develops and executes multi-product global regulatory CMC strategies for investigational... ...Biology, Chemistry, Pharmacy, Regulatory Affairs for Drugs, Biologics or Medical Devices)... ...and ICH) guidelinesReports to: Executive Director, CMC RegulatoryLocation: San Carlos, CA...$220k - $270k
Senior Director/ Director, CMC Regulatory Affairs ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients’ lives... .... Proven ability to manage multiple tasks and associated deadlines. Compensation The anticipated salary range...Currently hiring$189.7k - $237.1k
Position Summary: Director, Regulatory CMC. Develop and execute global regulatory CMC strategies supporting clinical development, marketing approvals... .... Primary Responsibilities: Manage CMC regulatory affairs for marketed products and compounds in development per US and...Worldwide- Enigma Search is seeking a seasoned Director of Regulatory Affairs to shape regulatory strategy for innovative programs. You will lead global submissions, interact with health authorities, and partner with executive leadership to align regulatory plans with corporate aims...
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...everything that we do on behalf of patients with cancer. Position Summary Reporting to the Executive Director, CMC Regulatory Affairs, the Senior Manager or Associate Director of CMC Regulatory Affairs will lead and participate in regulatory activities associated with...Temporary workCasual workLocal areaWorldwideFlexible hours- Lyell Immunopharma is seeking a Director of Regulatory Affairs/Global Regulatory Lead to define, develop, and execute global regulatory strategies for CAR-T programs from early development through licensure and lifecycle management. You will serve as the primary regulatory...
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