Associate Director, Regulatory Project Manager
$171k - $223kDenali Therapeutics
Neurodegenerative 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. This role drives the operational backbone of Denali's regulatory strategy, ensuring that every drug candidate's path from IND/CTA through BLA/NDA/MAA stays on track, on time, and aligned across functions. Acting as a trusted cross-functional partner to Regulatory Program Managers, Medical Writing, Regulatory Operations, and development SMEs, this individual anticipates risk before it becomes delay and translates complex, shifting priorities into clear, actionable plans. The role shapes how Regulatory Affairs plans and resources its work, contributing directly to Denali's ability to bring novel therapies for neurodegenerative disease to patients faster. Key Accountabilities / Core Job Responsibilities: Leads development and management of regulatory activity timelines across the portfolio, spanning regulatory documents, health authority interactions, and submissions, anticipating downstream risk and adjusting strategy as program priorities shift. Partners with Regulatory Program Managers and Program Directors to align regulatory timelines with corporate and program-level goals, resolving competing priorities across programs. Manages external partnerships with vendors. Drives timely delivery from cross-functional SMEs, applying judgment to unblock complex, ambiguous issues that don't have a standard playbook. Supports cross-functional health authority interaction and filing team project needs, owning risk identification, mitigation planning, and timeline impact assessment in partnership with Filing Team/Health Authority Interaction Leads. Owns regulatory timeline templates and resourcing models, shaping Regulatory Affairs' long-range and annual budget forecasting. Drives regulatory initiatives and/or represents Regulatory Affairs on strategic cross-functional initiatives. Mentors and provides technical direction to junior regulatory project management staff on complex filings, without formal supervisory responsibility. Qualifications/Skills: Typically requires a minimum of 12 years of related experience with a Bachelor's degree; or 10 years and a Master's degree; or a PhD with 7 years experience; or equivalent experience - and 5+ years of project/program management experience Typically requires demonstrated experience leading regulatory project management across INDs/CTAs and marketing applications; rare disease and/or complex filing experience preferred. Proficiency in Smartsheet or comparable project/resource management software. Demonstrated ability to lead cross-functional teams and influence senior stakeholders without direct authority. Strong track record identifying risk proactively and driving resolution across ambiguous, multi-stakeholder problems. Salary Range: $171,000.00 to $223,000.00 . 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: 401k healthcare coverage ESPP broad range of other benefits 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
$171k - $223k
...operational backbone of Denali's regulatory strategy, ensuring that every... ...to Regulatory Program Managers, Medical Writing, Regulatory... ...Program Managers and Program Directors to align regulatory timelines... ...interaction and filing team project needs, owning risk identification...SuggestedLocal areaShift work- ...three days per week on average. Position Summary The Associate Director, Regulatory Affairs Project Planning & Coordination is responsible for developing,... ...risk identification, and proactive planning Develop and manage a clinical trial public disclosure tracker and lead...SuggestedWork at officeLocal areaRemote workNight shift3 days per week
$164k - $204k
...insights to redefine complex diseases and identify new targets and drugs. To enable this vision we are seeking an Sr. Manager (Associate Director) of Project and Portfolio Management who will help our project teams to discover and advance exciting drug candidates into the...SuggestedWork at officeLocal areaRemote workHome officeFlexible hours3 days per week$120.2k - $223.2k
The PositionCommercial Regulatory Affairs (CORA) is part of the... ...Global Legal Pharma Department.Associate Program Directors of Commercial Medical... ...Program Directors and their managers. They are experienced... ...products, business areas, and projects, providing sound...SuggestedFull timeWork experience placementLocal areaWorldwideRelocation package$198k - $257k
...employees. Job Description Primary Function: The Associate Director, Regulatory Affairs supports the development and execution of clinical... .... Regulatory Submissions: Plan, prepare, and manage Investigational New Drug (IND) applications and other pre-...SuggestedWork at officeWorldwideRelocation package$200.7k - $234.15k
...cardiac muscle dysfunction. Reporting to the Executive Director, Regulatory Affairs, the Associate Director, Regulatory Affairs, is responsible for hands... ...health authority interactions ~ Proven ability to manage multiple priorities and work effectively across teams,...$170k - $230k
Position Title: Associate Director, Regulatory Strategy Reports To: Executive Director, Regulatory Department: Regulatory Location: South San Francisco... ...skills and attention to detail with the ability to manage multiple priorities Effective communication skills and ability...$210k - $240k
...individual will also oversee project management including timelines, budgets,... ...documentation, and may assist with regulatory filings. This position reports to Senior Director, CMC Program Management and is... ...anticipated salary range for Associate Director level candidates who...Full timeH1b$215.54k - $260.82k
Associate Director, Clinical Regulatory page is loaded## Associate Director, Clinical Regulatorylocations: South... ...Health Authority interactions, project team support, regulatory intelligence... ...guidelines, and Denali SOPs* Develops, manages, and mentors junior regulatory...Work experience placementLocal area- ...to be an equal opportunity employer and will consider all qualified applicants for employment. Position: Senior Manager / Associate Director, Regulatory Affairs Location: South San Francisco, CA Job Id: 357 # of Openings: 1 Senior Manager / Associate Director, Regulatory...Work at officeShift work
$180k - $210.5k
...executes multi-product global regulatory CMC strategies for... ...regulatory CMC submissions. Manages interactions with Health Authorities... ...throughout developmentLeads projects with cross-functional teams and... ...guidelinesReports to: Executive Director, CMC RegulatoryLocation: San...$160k - $180k
...The Associate Director, IT Compliance is responsible for organising, leading... ...activities, and regulatory compliance guidance for GxP... ...audit, certification, risk management and continuous improvement... ...cloud services and technology projects. Improved audit evidence...Full timeContract workWorldwideFlexible hours- Initial Therapeutics, Inc. is seeking an Associate Director, Quality Management Systems (QMS) in South San Francisco. This role involves leading the... ...implementing quality policies, and ensuring compliance with regulatory standards in the development of new cancer therapies....
$205k - $225k
...Associate Director, Regulatory Affairs Advertising and Promotion Foster City Mission Mirum... ...develop strategies and timelines, and managing internal team discussions to support... ...to work simultaneously on multiple projects with tight timelines. Excellent communication...Work at officeLocal area- Cytokinetics, a specialty cardiovascular biopharmaceutical company, seeks an Associate Director of Regulatory Affairs to lead regulatory activities across development stages and interact with health authorities. You will drive strategies for assigned programs, prepare...
- Ultragenyx Pharmaceutical is seeking an Associate Director of Quality Assurance who will lead the creation and evolution of QA strategies,... ...improvements. The position requires proven experience in audits, regulatory inspections, and cross-functional collaboration, with a...
- Kardigan is looking for an Associate Director, Regulatory Strategy to support regulatory strategies and ensure high-quality deliverables. You will collaborate cross-functionally and manage submission timelines while reporting to the Executive Director, Regulatory. The ideal...
- ...marginalization. Position Summary : The Associate Director of Compliance Systems is responsible... ...improvements. Cross-Functional Project Leadership Partner across... ...integrated into standard operations. Manage organizational change projects around compliance...Full timeContract workWork at office
- ...talent, we are open to remote.As an Associate Director, Quality Assurance Compliance at... ...and Logistics (Foster City):Manages the logistics to support regulatory inspections at GSI Foster City including... ...activities by partnering with project teams to evaluate inspection...Full timeFor contractorsWork at officeLocal areaRemote work
$190k - $230k
...SummaryReporting to the Senior Director of Medical Affairs, this position will be responsible for managing activities essential to the... ...tracking of Medical Affairs projects, with a primary focus on the... ...processes, and tools to ensure regulatory compliance, operational efficiency...Work at officeRemote workFlexible hours$230k - $240k
...Position Description:Calico is seeking an Associate Director, Medical Writing to provide... ...process of high quality clinical and regulatory documents, in compliance with applicable... ...This role will function as a strong project manager and technical leader with demonstrated...Work at office$215k - $265k
...breakthroughs.Position Description:Calico is seeking a highly motivated Associate Director/Director to join our Translational Medicine team. The... ...serve as translational physiology representatives on project teamsContribute to the development of preclinical strategies...$122.54k - $128.99k
...Job Summary: The Associate Director of Compliance ensures regulatory and compliance requirements are met for all properties owned and/or managed by Chinatown Community Development Center. The Associate Director ensures prompt contract renewals with various agencies...Full timeContract workLocal areaWork from homeMonday to Friday$186k - $220k
...location.Position Summary:The Associate Director of Clinical Operations... ...execution and compliance with regulatory standards. This senior-... ...functional study teams, vendor management, and direct contributions... ...investigator meetings and project team meetings. Act as a clinical...Contract workRemote work$193k - $246k
...inflection point.insitro is seeking an (Associate) Director, Drug Product Operations to lead drug... ...working closely with other CMC roles, Regulatory, and Clinical Operations. Because our... ...Oversight: Drive day-to-day technical management of CDMO relationships to keep programs...Work at officeLocal areaRemote workHome officeFlexible hours3 days per week$176k - $220k
...The Role We are looking for an Associate Director, Compliance Issue Management to own how Flex identifies, resolves... ...documented and remediated, and project‑manage resolution across teams that... ...accuracy, audit‑ability, or regulatory defensibility. This role is right...Full timeLocal areaRelocation packageFlexible hours2 days per week3 days per week$265k - $285k
...GroupContact: ApplicationsEmail: ****@*****.*** include: Provides regulatory leadership in support of the development, registration, and life-cycle management of products by collaborating cross-functionally with Clinical Development, Clinical...$275k - $280k
...Position Description: Calico is seeking a Regulatory Director that will be responsible for, in... ...key updates to senior leadership and project teams, anticipating changes in the regulatory... ...etc.)Direct experience authoring and managing (or oversight of others) substantial...Full time$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...$143k - $175k
...structure, visibility, and execution discipline to a growing Regulatory function at Maze. At Maze, we're on a mission to uncover... ...we're looking for someone who shares that spirit. As our Project Manager, Regulatory Affairs, you'll play a key role in supporting regulatory...
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