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Associate Director, Clinical Quality

Denali TherapeuticsSouth San Francisco, CA

$193,638 - $224,270 / year

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Overview

Schedule
Full-time
Career level
Executive
Compensation
$193,638-$224,270/year
Benefits
Health Insurance
401k Matching/Retirement Savings

Job Description

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.

The Associate Director, GCP Clinical Quality will play a key role in ensuring the successful execution of Denali's clinical trials by delivering strategic quality oversight and fostering a culture of compliance and continuous improvement. This position partners cross-functionally across study teams, site leadership, and external partners to uphold high standards of GCP compliance, support inspection readiness, and contribute to the advancement of Denali's portfolio. The ideal candidate brings a proactive, solution-oriented approach to identifying quality risks, implementing corrective actions, and driving operational excellence across Clinical Development activities.

Key Accountabilities/Core Job Responsibilities:

  • Serve as a GCP Quality team member on Study Execution Teams (SETs) and deliver a cohesive strategic GCP framework across Denali clinical trials.

  • Partner with the Zurich Site Lead and cross-functional leaders to drive site growth, operational excellence, and portfolio advancement.

  • Monitor, analyze, and report on quality issues; provide strategic, risk-based guidance in line with GCP regulations and industry standards.

  • Identify quality and compliance gaps, recommend solutions, and support CAPA development and root cause analysis.

  • Participate in the evaluation, selection, and oversight of CROs and clinical vendors to ensure quality standards are met.

  • Foster collaboration across internal teams and external partners to maintain systems and processes aligned with regulatory requirements.

  • Support inspection readiness activities, including preparation for regulatory agency inspections, audits, and vendor assessments.

  • Contribute to the design, implementation, and continuous improvement of GCP Quality Systems, SOPs, and the overall Quality Management System (QMS).

  • Perform QA reviews of essential clinical trial documents and assist in the implementation of internal GCP QA processes and tools.

  • Represent Clinical Quality Assurance (CQA) in internal initiatives, champion a culture of compliance, ethics, and patient safety, and ensure GCP adherence across clinical programs.

Qualifications/Skills

  • Bachelor's Degree and 7+ years experience, with 6+ working in GCP QA .

  • Early phase study support experience desirable.

  • Working knowledge of ICH E6 GCP guidelines, FDA Code of Federal Regulations, and other global applicable laws and regulations

  • Experience applying risk-based methodology and working within the QMS framework

  • Knowledge of clinical trial systems and processes

  • Attention to detail and accuracy in work, while delivering on deadline

  • Excellent verbal, written communication, and interpersonal skills

  • Work according to procedures, guidelines and regulations

  • Critical thinker with ability to synthesize information from multiple sources and apply to problem-solving

  • Positive, self-starter and thrives under pressure

  • Able to work across multiple projects and prioritize tasks as required

Salary Range: $193,638.00 to $224,270.00 . 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.

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FAQs About Associate Director, Clinical Quality Jobs at Denali Therapeutics

What is the work location for this position at Denali Therapeutics?
This job at Denali Therapeutics is located in South San Francisco, CA, according to the details provided by the employer. Some roles may also include multiple work locations depending on the requirement.
What pay range can candidates expect for this role at Denali Therapeutics?
Candidates can expect a pay range of $193,638 and $224,270 per year.
What employment applies to this position at Denali Therapeutics?
Denali Therapeutics lists this role as a Full-time position.
What experience level is required for this role at Denali Therapeutics?
Denali Therapeutics is looking for a candidate with "Executive" experience level.
What benefits are offered by Denali Therapeutics for this role?
Denali Therapeutics offers following benefits: Health Insurance and 401k Matching/Retirement Savings for this position. Actual benefits may vary depending on the employer's policies and employment terms.
What is the process to apply for this position at Denali Therapeutics?
You can apply for this role at Denali Therapeutics either through Sonara's automated application system, which helps you submit applications 10X faster with minimal effort, or by applying manually using the direct link on the job page.