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Vp Regulatory Risk Jobs (NOW HIRING)

Codera

Vice President, Clinical Development

San Diego, CA · On-site

$345K - $375K/yr

... risk management * Oversee biometrics and medical writing to ensure all clinical and nonclinical ... Collaborate with the Vice President, Regulatory Affairs in the development and execution of ...

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How much do vp regulatory risk jobs pay per year?

As of Sep 13, 2026, the average yearly pay for vp regulatory risk in the United States is $111,556.00, according to ZipRecruiter salary data. Most workers in this role earn between $90,000.00 and $129,000.00 per year, depending on experience, location, and employer.

What are the most commonly searched types of Regulatory Risk jobs?

The most popular types of Regulatory Risk jobs are:

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Infographic showing various Vp Regulatory Risk job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 86% Full Time, 9% Part Time, and 3% Contract. Highlights an 90% Physical, 4% Hybrid, and 6% Remote job distribution, with an average salary of $111,556 per year, or $53.6 per hour.

Senior Director/Executive Director, Global Regulatory Lead

Bothell, WA • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

$226K - $270K/yr

Other

Posted 14 days ago

Job description

Position Overview

As the Global Regulatory Lead, you will develop and execute global regulatory strategies to maximize global regulatory success across complex and/or multiple oncology programs. You will report to the Vice President, Regulatory Affairs.

Responsibilities
  • Define and implement global regulatory strategies that adapt to changing regulatory and business needs.
  • Communicate key developments to project teams and stakeholders; anticipate risks and devise solutions.
  • Lead the Global Regulatory Team through coaching and mentoring.
  • Collaborate with regional regulatory leads and vendors to ensure compliance with local regulations for global submissions.
  • Advocate for regulatory positions in governance and cross-functional committees with internal and external partners.
  • Identify regulatory risks and opportunities; develop mitigation strategies to enhance success rates.
  • Ensure timely preparation and submission of regulatory submissions (e.g., INDs, BLAs, NDAs) while maintaining regional and global compliance.
  • Act as the primary contact with global health authorities and lead FDA meetings.
  • Monitor industry trends and regulatory changes and adapt strategies to mitigate impacts.
Qualifications
  • Bachelor's degree in a relevant scientific discipline.
  • 10+ years of experience in global regulatory affairs in pharma/biotech (or equivalent).
  • Proven success leading regulatory submissions and obtaining approvals in major markets.
  • Oncology therapeutics experience strongly preferred.
Knowledge and Skills
  • Direct experience leading regulatory submissions and health authority interactions (FDA, EMA, and others).
  • Disciplined regulatory risk management and oncology therapeutic area expertise.
  • Highly collaborative, open communication; strong analytical, organizational, and time management skills.
  • Comfortable working with small teams under evolving scenarios and tight deadlines.
  • Detail-minded yet flexible; manage multiple projects and reprioritize quickly.

Washington State Pay Range: $226,000 - $270,000 USD

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