Revolution Medicines

Associate Director, Commercial Regulatory Affairs

Revolution Medicines$186K — $233K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in a relevant field with 10+ years relevant experience.
  • 5-7 years of relevant promotional regulatory affairs experience in the biotech or pharmaceutical industry for the US market.
  • Strong understanding of FDA regulatory requirements governing promotional activities.
  • Track record of influencing cross-functional decisions and operating with sound regulatory judgment.
  • Excellent communication skills and ability to work collaboratively across teams.

Responsibilities

  • Serve as a primary or secondary regulatory advertising and promotion reviewer.
  • Manage regulatory submissions of promotional materials to health authorities as required.
  • Interpret evolving regulatory requirements and guide commercial strategy accordingly.
  • Train and advise cross-functional teams on compliance and best practices.
  • Monitor the US regulatory promotional environment through continuous review of guidelines and attendance at industry meetings.
  • Ensure updates in US Prescribing Information are accurately reflected in advertising materials.
  • Participate in the development and maintenance of MLR operational objectives and procedures.

Benefits

  • Hybrid work schedule offering flexibility with potential for remote work.
  • Robust equity awards as part of the total rewards program.
  • Strong benefits package that supports well-being and work-life balance.
  • Significant learning and development opportunities to enhance skills.
Full Job Description
The Opportunity:

Revolution Medicines is seeking an Associate Director, Commercial Regulatory Affairs to partner closely with the cross-functional teams to ensure that all promotional and medical communication strategies are compliant with applicable regulations, industry standards, and internal policies. This role will help enable successful product commercialization while upholding regulatory integrity and scientific accuracy.

As part of the Regulatory Affairs function, the Associate Director will work under supervision to provide strategic regulatory advice on advertising/promotion and medical materials to the US organization for assigned products in accordance with business goals and objectives, FDA regulations/guidances, pharma guidelines, and company policy.

The position can be based at our Redwood City, CA site in a hybrid work schedule (preferred) or remote-based with quarterly and as needed travel.

Required Skills, Experience and Education:
  • Serves as a primary or secondary regulatory advertising and promotion reviewer for assigned products on MLR teams with oversight.
  • Manage regulatory submissions of promotional materials as required (e.g., FDA Form 2253) and interact with health authority stakeholders when applicable.
  • Interpret evolving regulatory requirements and enforcement trends to proactively guide commercial strategy and risk assessments.
  • Train and advise cross-functional teams on commercial regulatory compliance, MLR process and best practices.
  • Monitors US regulatory promotional environment by reviewing regulatory promotional guidelines, untitled and warning letters to pharmaceutical/biotech companies published by OPDP or APLB, and by attendance of major FDLI, DIA and other industry meetings.
  • Ensures that changes in US Prescribing Information are reflected in current promotion and advertising.
  • Participate in the development and maintenance of MLR operational objectives, policies, and procedures.
  • Bachelor's Degree in a relevant field with 10+ years relevant experience.
  • 5-7 years of relevant promotional regulatory affairs experience in the biotech or pharmaceutical industry for the US market.
  • Strong understanding of FDA regulatory requirements governing promotional activities and experience managing promotional submissions and reviews.
  • Strong, current understanding of scientific exchange and pre-approval discussions; ability to unpack and deploy these concepts in practice.
  • Track record of influencing cross-functional decisions and operating with sound regulatory judgment.
  • Excellent communication skills and ability to work collaboratively across teams.
  • Collaborative and solution-oriented mindset and approach.
  • Exemplary compliance ethics and high concern for standards.

Preferred:
  • Advanced degree in a relevant field.
  • Experience in oncology therapeutic areas.
  • Experience with product launches.

#LI-Hybrid #LI-JC1

The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.

Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.

Base Pay Salary Range

$186,000-$233,000 USD

We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message.

Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address.

If you believe you've been contacted by someone impersonating a Revolution Medicines recruiter, please report it to [email protected] so we can share these impersonations with our IT team for tracking and awareness.

About Revolution Medicines

Revolution Medicines is a clinical-stage precision oncology company focused on developing targeted therapies to inhibit elusive frontier targets within notorious growth and survival pathways, with particular emphasis on RAS and mTOR signaling pathways. The company's proprietary platform enables the discovery and development of small molecules that bind covalently to proteins. Revolution Medicines was founded in 2014 and is headquartered in South San Francisco, California.
Learn more about Revolution Medicines
Size
201 employees
Market Cap
$2.1 billion
Industry
Net Income
-$108.1 million
Revenue
$42.9 million
NASDAQ

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