Associate Director, CMC Program Mgmt

Posted 15 Days Ago
Be an Early Applicant
South San Francisco, CA, USA
In-Office
159K-207K Annually
Expert/Leader
Biotech
The Role
Lead and manage CMC strategies, timelines, budgets, and vendor relationships across drug development stages. Oversee CRO/CMO selection and outsourced manufacturing, drive cross-functional CMC teams, identify risks and mitigations, and report status and forecasts to senior management to ensure timely regulatory submissions and commercialization readiness.
Summary Generated by Built In

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.

Denali Therapeutics is seeking to recruit a leader who will be responsible for organizing and managing CMC strategies, deliverables, and timelines for Denali’s programs, including oversight of contract manufacturing organizations. As a member of the CMC Program Management group, this position is responsible for ensuring timely and optimal decision making across the CMC portfolio from the research phase through all phases of development, including approval (NDA, BLA, MAA) and commercial, working closely with our technical leaders, Program Directors, and cross-functional project teams to successfully integrate CMC deliverables into the overall project timelines.

Key Accountabilities/Core Job Responsibilities

  • Organize, manage, and drive CMC strategies, plans, and deliverables for drug candidates from the research, pre-IND, and first-in-human testing phases to all later phases of development, including pivotal Phase 2/3 studies and NDA/MAA/BLA submissions

  • Manage CRO/CMO vendor selection process and serve as a point of contact for CROs and CMOs for outsourced CMC projects as well as early stage biotherapeutics requiring large scale material production

  • Facilitate, manage, and lead internal CMC project teams

  • Establish and maintain CMC project timelines and budgets and track CMC deliverables and timelines and ensure the CMC strategies and plans are incorporated into the overall project plans

  • Proactively outline risks and mitigations and communicate risks and issues to CMC teams, project teams, and senior management

  • Provide regular updates to senior management on project status, timelines, risks, and forecasting for future CMC project needs

  • Collaborate with technical leaders, Program Directors, and cross-functional project teams to develop and execute on drug development strategies and plans

Qualifications/Skills

  • Typically requires a BA or BS degree in Science, Mathematics, Engineering, or a related scientific discipline, with 12+ years of relevant biotech/pharmaceutical/CMO CMC experience.(or Master’s degree with 10+ years of experience)

  • An advanced degree and CMC Experience with novel constructs (e.g. bi-specifics, enzyme fusions) is preferred.

  • Experience managing CMC activities at CROs/CMOs required

  • Drug Substance and Drug Product GMP experience required

  • Command of project management practices and software

  • Thorough understanding of the overall drug development process

  • Excellent leadership, interpersonal skills and demonstrated ability to build effective working relationships and partnerships with internal team members and collaborators at CROs/CMOs

  • Experience in effectively working through high-pressure situations; excellent conflict management skills.

  • Drive to take ownership and responsibility in ensuring the success of the projects and deliverables. Results- and detail-oriented.

Salary Range: $159,000.00 to $207,000.00 .  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 a 401k, healthcare coverage, ESPP and a broad range of other benefits. Learn more at https://www.denalitherapeutics.com/careers

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.

Skills Required

  • BA or BS in Science, Mathematics, Engineering, or related discipline with 12+ years relevant biotech/pharmaceutical/CMO CMC experience (or Master's with 10+ years).
  • Experience managing CMC activities at CROs/CMOs.
  • Drug Substance and Drug Product GMP experience.
  • Command of project management practices and software.
  • Thorough understanding of the overall drug development process.
  • Excellent leadership and interpersonal skills; ability to build effective internal and external partnerships.
  • Experience working effectively under high-pressure situations and strong conflict management skills.
  • Ability to take ownership and drive project success; results- and detail-oriented.
  • Advanced degree and CMC experience with novel constructs (e.g., bispecifics, enzyme fusions).

Denali Therapeutics Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Denali Therapeutics and has not been reviewed or approved by Denali Therapeutics.

  • Healthcare Strength Health coverage is described as strong, with the employee premium covered in certain cases. Core medical benefits are consistently highlighted in public materials and postings.
  • Retirement Support A 401(k) plan with employer safe-harbor contributions is confirmed by company materials. Contributions are described as being deposited each payroll, signaling dependable support for retirement savings.
  • Equity Value & Accessibility An employee stock purchase plan is offered and enhanced by a “Cashless Participation” feature through a vendor partnership, improving ease of participation. Equity programs are also referenced in job postings and filings.

Denali Therapeutics Insights

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The Company
HQ: South San Francisco, CA
437 Employees
Year Founded: 2015

What We Do

Denali Therapeutics is dedicated to defeating neurodegenerative diseases by breaking through historical barriers in scientific research and clinical development in order to deliver safe and effective medicines to patients and families. Our scientific approach is based on three core principles: rigorous assessment of genetic targets, engineering brain delivery, and using biomarkers to guide development. Our team thrives in a work environment that is scientifically driven, impact-focused, supportive, and collaborative. Our ability to have a positive impact on people’s lives is directly related to the trust we have in each other and our ability to unify our diverse backgrounds and experience behind our purpose to defeat degeneration.

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