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
$120.2k - $223.2k
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$200.7k - $234.15k
## Associate Director, Regulatory AffairsApplyremote type: Hybridlocations: South San Francisco, Californiatime type: Full timeposted on: Posted... ...dysfunction.Reporting to the Executive Director, Regulatory Affairs, the Associate Director, Regulatory Affairs, is...Suggested- ...to manage, evaluate, and complete regulatory projects consistent with company goals... ...the company and industry are met. The Associate Director will also manage regulatory aspects of... ...working as a Project Lead in Regulatory Affairs, leading multiple FDA interactions....Suggested
$198k - $257k
...2, the Company has a global team of approximately 2000 employees. Job Description Primary Function: The Associate Director, Regulatory Affairs supports the development and execution of clinical regulatory strategies and regulatory development activities for...SuggestedWork at officeWorldwideRelocation package$275k - $280k
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...expanding organization, we seek a strategic and hands‑on Associate Director, CMC Regulatory who will be responsible for executing CMC regulatory... ...experience with 5+ years of experience of global CMC regulatory affairs. Experience in CMC related global submissions (IND, IMPD...Work experience placement- ...Thursday. For non-local talent, we are open to remote.As an Associate Director, Quality Assurance Compliance at Gilead you will have the following... ...Logistics (Foster City):Manages the logistics to support regulatory inspections at GSI Foster City including notification...Full timeFor contractorsWork at officeLocal areaRemote work
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$33 - $38 per hour
...professionals and gain practical skills in audit support, data analysis, and licensee management. This hybrid role reports to the Director of Global Compliance and is based at Via LA's headquarters in San Francisco, California. The intern is required to work on-site at...Hourly payWork experience placementInternshipWork at officeLocal areaWorldwideFlexible hours3 days per week$230k - $240k
...medical breakthroughs.Position Description:Calico is seeking an Associate Director, Medical Writing to provide leadership and functional... ...leading the review/approval process of high quality clinical and regulatory documents, in compliance with applicable guidelines and...Work at office$215k - $265k
...inspiring and exciting place to catalyze and enable medical breakthroughs.Position Description:Calico is seeking a highly motivated Associate Director/Director to join our Translational Medicine team. The successful candidate will lead our preclinical in vivo physiology...$276k - $414k
Job Title: Executive Director, Regulatory Affairs Strategy - Cell Therapy Available locations: Gaithersburg, MDBoston, MASouth San Francisco, CASanta Monica, CAIntroduction to role: Are you ready to set the global regulatory direction for first-in-class cell therapies...Hourly payFull timeTemporary workWork at officeWorldwideFlexible hours3 days per week$275k - $280k
...pipeline, together create an inspiring and exciting place to catalyze and enable medical breakthroughs.Position Description:The Director of Regulatory CMC will lead the development and execution of global CMC regulatory strategies for our pipeline of small molecules and...$302.01k - $390.83k
...together.Job DescriptionPOSITION OVERVIEW:The Executive Director, Head of Precision Medicine Regulatory is responsible for defining and leading enterprise-... ...closely with the Vice President, Global Regulatory Affairs Oncology and Precision Medicine, and collaborate with...Full timeFor contractorsWork at officeLocal areaFlexible hours$138.3k - $256.8k
...integrity and creativity while boldly pursuing answers to the world’s most complex health challenges and transforming society.Public Affairs & Access (PAA) is a multi-disciplinary organization that includes Corporate Communications; Policy, Evidence & Access Strategy;...Full timeContract workWork experience placementWork at officeLocal areaRelocation package3 days per week$195.5k - $272.5k
...seeking an a highly motivated, self-driven and enthusiastic Director of Regulatory CMC accountable for ensuring all assigned products have a... ...Technical Operations (CMC) functional groups and Regulatory Affairs department to plan and lead high quality regulatory submissions...Full timeWork at officeWork visa3 days per week$140k - $214k
...is seeking a Senior Manager, Regulatory CMC to join an experienced,... ...Manager will report to the Senior Director of Regulatory CMC and will... ....Represent Regulatory Affairs on cross-functional project... ...prioritize regulatory activities and associated resources, ensuring they are...Contract workFor contractorsFlexible hours$280k - $310k
...other individuals who embody our values: care, be real, get it done, and have fun, seriously.POSTION SUMMARYThe Senior Director, Regulatory Affairs CMC is a position requiring a strong leader who will provide strategic and operational leadership, and who will ensure the...Local area$220.6k - $275.7k
...three days per week on average. Position Summary The Senior Director, Regulatory Operations provides strategic and operational leadership for... .... This role is a key member of the Global Regulatory Affairs Leadership Team and plays a critical role in driving operational...Full timeWork at officeLocal areaRemote workWorldwideNight shift3 days per week$195k - $200k
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