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Regulatory Project Jobs in California (NOW HIRING)

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Regulatory Project information

See California salary details

$16

$52

$88

How much do regulatory project jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for regulatory project in California is $52.01, according to ZipRecruiter salary data. Most workers in this role earn between $37.19 and $67.56 per hour, depending on experience, location, and employer.

What is a regulatory project manager?

A Regulatory Project Manager is a professional who oversees and coordinates regulatory activities for organizations, particularly in industries like pharmaceuticals, biotechnology, and medical devices. Their primary responsibility is to ensure that products comply with all relevant regulations and standards, managing submissions to regulatory authorities and tracking progress through the approval process. They collaborate with cross-functional teams, develop regulatory strategies, and keep up-to-date with changing regulations to ensure successful product launches. Effective Regulatory Project Managers possess strong project management, communication, and analytical skills.

What are the key skills and qualifications needed to thrive as a regulatory project manager?

To thrive as a Regulatory Project Manager, you need a solid understanding of regulatory requirements, project management principles, and industry standards, often supported by a degree in life sciences or a related field. Familiarity with regulatory submission systems, project management tools like MS Project, and certifications such as PMP or RAC are highly valued. Strong organizational, communication, and problem-solving skills help manage cross-functional teams and adapt to evolving regulations. These skills ensure timely regulatory submissions, compliance, and effective coordination throughout complex projects.

How does a regulatory project manager typically collaborate with cross-functional teams during the product development lifecycle?

A Regulatory Project Manager works closely with teams such as R&D, Quality Assurance, Clinical, and Marketing to ensure that all regulatory requirements are met throughout the product development process. They facilitate communication between departments, coordinate the preparation and submission of regulatory documents, and help troubleshoot compliance issues as they arise. This role requires effective project management and strong interpersonal skills to align team efforts with regulatory timelines and standards, ensuring a smooth path to product approval.

What is the difference between Regulatory Project vs Regulatory Affairs Specialist?

AspectRegulatory ProjectRegulatory Affairs Specialist
CertificationsOften requires project management and regulatory certificationsTypically holds certifications like RAC or RA
Work EnvironmentFocuses on managing specific regulatory projects within teamsHandles ongoing regulatory compliance and submissions
Employer & Industry UsageCommon in pharmaceutical, biotech, and medical device companiesWidely used across similar industries for compliance roles

While both roles operate within regulatory frameworks, Regulatory Project managers oversee specific projects ensuring timely compliance, whereas Regulatory Affairs Specialists handle continuous regulatory activities and submissions. The roles often collaborate but differ in scope and focus.

What are the most commonly searched types of Regulatory Project jobs in California?

The most popular types of Regulatory Project jobs in California are:

Infographic showing various Regulatory Project job openings in California as of August 2026, with employment types broken down into 90% Full Time, 7% Part Time, and 3% Contract. Highlights an 82% Physical, 5% Hybrid, and 13% Remote job distribution, with an average salary of $108,191 per year, or $52 per hour.

Associate Director, Regulatory Project Manager

Denali Therapeutics

South San Francisco, CA • On-site

$171 - $223/hr

Other

Medical, Retirement

Posted 8 days ago


Job description

## Associate Director, Regulatory Project ManagerApplylocations: South San Franciscotime type: Full timeposted on: Posted 4 Days Agojob requisition id: R-1627Neurodegenerative 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 a 401k, healthcare coverage, ESPP and a broad range of other benefits. Learn more at https://www.denalitherapeutics.com/careersThis 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. #J-18808-Ljbffr