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Vice President Regulatory Jobs (NOW HIRING)

Responsibilities / Position overview The Vice President, Regulatory Strategy is a senior enterprise leader who combines deep regulatory technical expertise with proven consulting and biopharma ...

Responsibilities / Position overview The Vice President, Regulatory Strategy is a senior enterprise leader who combines deep regulatory technical expertise with proven consulting and biopharma ...

$170.50K - $225.10K/yr

Vice President, Regulatory Affairs - Permanent - San Francisco, CA Proclinical is seeking a Vice President, Regulatory Affairs for a rapidly growing and exciting clinical-stage biotechnology company ...

VP Regulatory Affairs

Cary, NC · On-site +1

$152.90K - $201.80K/yr

As a VP Regulatory Affairs at Allucent, you are responsible for assisting clients with the regulatory activities of drug, biologic or medical device product. About the role As the VP Regulatory ...

VP Regulatory Affairs

Cary, NC · On-site +1

$139K - $183.40K/yr

As a VP Regulatory Affairs at Allucent, you are responsible for assisting clients with the regulatory activities of drug, biologic or medical device product. About the role As the VP Regulatory ...

VP Regulatory Affairs

Cary, NC · Remote

$153.50K - $202.70K/yr

As a VP Regulatory Affairs at Allucent, you are responsible for assisting clients with the regulatory activities of drug, biologic or medical device product. About the role As the VP Regulatory ...

VP Regulatory Affairs

Cary, NC · On-site +1

$139K - $183.40K/yr

As a VP Regulatory Affairs at Allucent, you are responsible for assisting clients with the regulatory activities of drug, biologic or medical device product. About the role As the VP Regulatory ...

$138.80K - $183.20K/yr

As a VP Regulatory Affairs at Allucent, you are responsible for assisting clients with the regulatory activities of drug, biologic or medical device product. About the role As the VP Regulatory ...

Vice President, Regulatory & Quality Remote (WFH) At Adaptive, we're Powering the Age of Immune Medicine. Our goal is to harness the power of the adaptive immune system to transform the way diseases ...

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Vice President Regulatory information

See salary details

$43.5K

$157.5K

$277.5K

How much do vice president regulatory jobs pay per year?

As of May 28, 2026, the average yearly pay for vice president regulatory in the United States is $157,532.00, according to ZipRecruiter salary data. Most workers in this role earn between $115,000.00 and $190,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Vice President Regulatory, and why are they important?

To thrive as a Vice President Regulatory, you need deep expertise in regulatory affairs, compliance, and industry-specific laws, usually demonstrated by an advanced degree and significant experience in regulatory roles. Familiarity with regulatory submission platforms, compliance management systems, and certifications such as RAC (Regulatory Affairs Certification) are commonly required. Outstanding leadership, strategic thinking, and strong interpersonal communication enable effective guidance of teams and collaboration with regulatory agencies. These skills ensure organizational compliance, minimize risk, and facilitate successful product approvals in highly regulated industries.

What are some typical challenges faced by a Vice President of Regulatory, and how can they be navigated effectively?

A Vice President of Regulatory often encounters challenges such as keeping pace with rapidly evolving regulations, aligning company operations with diverse global compliance standards, and managing cross-functional teams to ensure timely submissions. Proactive communication with regulatory agencies and strong collaboration across departments are essential for anticipating changes and addressing compliance gaps. Building a knowledgeable team and leveraging regulatory intelligence tools can greatly aid in navigating these complexities while minimizing risk to the organization.

What does a Vice President of Regulatory do?

A Vice President of Regulatory is responsible for overseeing an organization's compliance with laws and regulations relevant to its industry. They lead the development and implementation of regulatory strategies, ensure the company meets all legal requirements, and interact with regulatory agencies. This role often involves managing submissions, audits, and inspections, as well as keeping the organization informed about changes in regulatory policies. The VP of Regulatory plays a critical role in minimizing risks and supporting the company's business objectives through effective compliance management.

What is the difference between Vice President Regulatory vs Regulatory Manager?

AspectVice President RegulatoryRegulatory Manager
ResponsibilitiesStrategic oversight of regulatory compliance, policy development, and industry advocacy at executive levelManaging daily regulatory operations, ensuring compliance, and preparing documentation
Required CredentialsAdvanced degree (e.g., JD, MS), extensive regulatory experience, leadership skillsBachelor’s or Master’s degree, relevant regulatory experience
Work EnvironmentExecutive offices, cross-departmental collaboration, industry associationsRegulatory departments, compliance teams, project management

The Vice President Regulatory holds a senior leadership role focused on strategic regulatory initiatives, while the Regulatory Manager handles operational compliance tasks. Both roles require regulatory expertise, but the VP is more involved in policy and industry strategy, whereas the Manager manages day-to-day compliance activities.

What cities are hiring for Vice President Regulatory jobs? Cities with the most Vice President Regulatory job openings:
What are the most commonly searched types of Regulatory jobs? The most popular types of Regulatory jobs are:
What states have the most Vice President Regulatory jobs? States with the most job openings for Vice President Regulatory jobs include:
Infographic showing various Vice President Regulatory job openings in the United States as of May 2026, with employment types broken down into 10% As Needed, 84% Full Time, and 6% Part Time. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $157,532 per year, or $75.7 per hour.

Vice President Regulatory Affairs

Proclinical Staffing

San Francisco, CA

$176.70K - $233.30K/yr

Full-time

Posted 12 days ago


Job description

Vice President, Regulatory Affairs – Permanent – San Francisco, CA

Proclinical is seeking a Vice President, Regulatory Affairs for a rapidly growing and exciting clinical-stage biotechnology company based in the San Francisco Bay Area, California.

Primary Responsibilities:

In this role, you will lead global regulatory strategy and operations across the company's development pipeline. This individual will be responsible for developing and executing regulatory strategies, overseeing submission activities (INDs, CTAs, NDAs/BLAs/MAAs), and partnering with internal stakeholders and external agencies to advance programs through clinical development and regulatory review.

The position is based in the San Francisco Bay Area, California in a hybrid work environment.

Skills & Requirements:

  • Advanced degree (PhD, PharmD, MD, MS) or BS in a scientific discipline with 10+ years of regulatory affairs experience in the biotech/pharmaceutical industry, including 5+ years at the Director level or above.
  • Demonstrated success developing and executing global regulatory strategies and leading submissions across multiple stages of drug development.
  • Deep knowledge of US regulatory requirements (FDA), with experience in ex-US markets (e.g., EMA, Health Canada, MHRA) preferred.
  • Hands-on experience with INDs, CTAs, NDAs, BLAs, MAAs, and regulatory agency meeting preparations.
  • Familiarity with special regulatory designations and accelerated pathways.
  • Experience in a fast-paced biotech or small company environment; adaptable, proactive, and collaborative.
  • Proficiency in regulatory operations, including working with publishing vendors and eCTD submissions. Experience with RIMS tools is a plus.
  • Experience in immunology, dermatology, or rare diseases is a plus.

The Vice President, Regulatory Affairs will:

  • Lead the development and execution of US and global regulatory strategies to support the advancement of their investigational products from preclinical through late-stage development.
  • Serve as the regulatory lead on cross-functional project teams, providing regulatory guidance to ensure alignment with clinical, CMC, nonclinical, and corporate goals.
  • Oversee preparation, submission, and maintenance of high-quality regulatory documents (e.g., INDs, CTAs, amendments, briefing books, meeting requests, and responses to health authority queries).
  • Manage interactions with regulatory authorities (FDA and ex-US) including leading or supporting meeting preparations and correspondence.
  • Evaluate regulatory risks and provide mitigation strategies to support timely development and approvals.
  • Provide regulatory guidance on special designations (e.g., Orphan Drug, Fast Track, Breakthrough Therapy) and expedited pathways, as applicable.
  • Support regulatory activities related to CMC, nonclinical, and pharmacovigilance to ensure comprehensive submission packages.

If you are having difficulty in applying or if you have any questions, please contact Phu Huynh at (+1) 646-779-7961 or p.huynh@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.