Revolution Medicines

Senior Director, US Compliance

Revolution Medicines$288K — $331K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • J.D. from an accredited US law school and member in good standing of a US State Bar.
  • 10+ years of healthcare compliance experience in pharmaceuticals or biotechnology, preferably in-house.
  • In-depth understanding of US healthcare laws such as the Anti-Kickback Statute and False Claims Act.
  • Proven experience in designing and overseeing effective compliance programs including risk assessments and investigations.
  • Strong ability to build partnerships and collaborate across various levels of the organization.

Responsibilities

  • Provide practical compliance advice on regulatory requirements for healthcare community interactions.
  • Support the review and approval of promotional and nonpromotional materials and programs for compliance.
  • Advise on compliance with major healthcare laws and statutes, ensuring adherence.
  • Collaborate closely with Healthcare Law to align legal and compliance operations.
  • Identify compliance risks and assist in developing mitigation strategies.
  • Support compliance training, ensuring it is relevant to various business functions.
  • Prepare governance materials for Compliance Committee and monitoring compliance risks.

Benefits

  • Competitive cash compensation and robust equity awards.
  • Strong benefits package, including health and wellness initiatives.
  • Significant learning and development opportunities.
  • Promotes a culture of ethics and compliance.
Full Job Description
The Opportunity:

The Sr. Director, US Compliance will serve as a strategic compliance business partner across all business functions, reporting to the VP, US Compliance. This role is responsible for shaping compliance strategy and providing proactive compliance advice and counsel as the company prepares for future product commercialization. This role requires a firm understanding of pharmaceutical industry codes and regulations, healthcare laws, and compliance risk assessment and management, as well as a strong ability to advise on interactions with the healthcare community and other external stakeholders. The individual will play an integral part in ensuring company activities are conducted in accordance with applicable healthcare laws, regulations, industry codes, and internal policies while enabling business objectives in a compliant and ethical manner.

The Sr. Director will collaborate cross-functionally with Commercial, Medical Affairs, Clinical Development, Patient Advocacy, Legal, Regulatory, Finance, and other stakeholders to support the compliant execution of Revolution Medicines' business activities. This role requires the ability to balance operational execution with strategic leadership in a dynamic and evolving organization.

Key Responsibilities will include:

Product Launch and Healthcare Community Engagement Support
  • Provide timely, practical, and risk-based compliance advice and counsel on healthcare compliance and policy requirements related to Revolution Medicines interactions with the healthcare community, including disease education programs, promotional and nonpromotional activities, consulting engagements, advisory boards, external funding, patient assistance programs, patient advocacy group interactions, payer interactions, and other similar activities.
  • Support the review and approval of promotional and nonpromotional materials and patient engagement programs to ensure regulatory compliance.
  • Advise on compliance with False Claims Act, Anti-Kickback Statute (AKS), Foreign Corrupt Practices Act (FCPA), and state/federal transparency laws.

Collaboration with Healthcare Law
  • Partner closely with the Healthcare Law team to ensure consistency between legal interpretation and compliance operations.
  • Maintain a clear functional separation of responsibilities between Compliance and Healthcare Law.
  • Collaborate to deliver integrated, practical, and risk-appropriate guidance to internal clients - particularly within Commercial, Medical Affairs, Clinical Development, and Market Access functions.

Compliance Risk Assessments, Investigations, and Mitigation
  • Identify and escalate compliance risks, and support development of mitigation strategies.
  • Support compliance risk assessments related to commercial and medical activities, external stakeholder engagements, and other business activities.
  • Support investigations into potential compliance violations, ensuring timely, thorough resolution and corrective actions.
  • Support implementation of corrective and preventive actions resulting from monitoring or audit activities.

Training, Communications, and Compliance Program Support
  • Support operational execution of healthcare compliance policies and processes.
  • Develop and implement risk-based compliance training tailored to various business functions and levels within the organization.
  • Promote a culture of ethics and compliance through ongoing communications and awareness initiatives.
  • Collaborate with internal stakeholders to identify process improvements and enhance operational efficiency.
  • Participate in compliance monitoring, auditing, and remediation activities, as needed.

Governance & Reporting
  • Prepare materials and reporting for Compliance Committee and senior leadership.
  • Develop and implement policies, procedures, and controls designed to mitigate compliance risk while supporting business needs.
  • Assist with the development, management, and reporting of data analytics to manage compliance risks.
  • Contribute to the development of annual compliance work plans and strategic priorities.
  • Monitor evolving regulatory and industry developments and assess impact on company policies and practices.

Required Skills, Experience and Education:
  • J.D. from an accredited US law school and member in good standing of a US State Bar.
  • 10+ years of healthcare compliance experience in pharmaceuticals or biotechnology, with in-house compliance experience strongly preferred.
  • In-depth understanding of US healthcare laws, including Anti-Kickback Statute, False Claims Act, FDA promotional regulations, FCPA, and relevant industry guidance.
  • Experience in designing, implementing, and overseeing key elements of an effective compliance program, including risk assessments, investigations, and compliance business partnership.
  • Demonstrated ability to build strong partnerships and collaborate with internal and external partners at all levels of the organization.
  • Strategic and pragmatic compliance mindset with strong business acumen.
  • High ethical standards and sound judgment, and committed to fostering a culture of integrity, transparency, and continuous improvement.
  • Excellent leadership, communication, analytical, and problem-solving skills, with the ability to work collaboratively with legal, scientific, and business functions.
  • Strong presentation, organizational, and project management skills, capable of handling multiple high-priority projects simultaneously.
  • Team-oriented approach to work, and ability to lead through influence in a dynamic environment.

#LI-TS1 #LI-Hybrid

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

$288,000-$331,000 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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