Revolution Medicines

Senior Director, US Compliance

Revolution Medicines$244K — $305K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree required
  • 10+ years healthcare compliance experience in pharmaceuticals or biotechnology, preferably in-house
  • Deep understanding of US healthcare laws and compliance guidelines
  • Experience as a compliance business partner in pre-commercial contexts
  • Proven ability to build and maintain collaborative relationships across functions
  • Strong strategic mindset with business acumen and ethical judgment
  • Proficient in data analysis and risk prioritization, alongside solid project management skills

Responsibilities

  • Serve as strategic compliance advisor for various cross-functional teams
  • Conduct ongoing compliance risk assessments in the NSCLC sector
  • Represent Compliance in commercialization committees and decision forums
  • Provide compliance guidance on NSCLC initiatives
  • Design and deliver compliance training to NSCLC business teams
  • Develop and improve compliance policies and governance controls
  • Lead monitoring and auditing activities to mitigate compliance risks

Benefits

  • Hybrid work schedule based in Redwood City, CA
  • Access to competitive cash compensation
  • Robust equity awards
  • Extensive learning and development opportunities
  • Inclusive culture promoting ethics and accountability
Full Job Description
The Opportunity:

The Sr. Director, US Compliance will serve as the lead compliance business partner in support of the company's planned US commercialization activities for non-small cell lung cancer (NSCLC). The Sr. Director will partner with a range of business functions, serve as a trusted resource for compliance guidance, and ensure launch teams successfully navigate the compliance landscape. This role requires a firm understanding of pharmaceutical best practices and industry requirements, as well as the passion and ability to build relationships with a diverse set of teams all working to revolutionize treatments for patients. This position will report to the VP, US Compliance.

This position will be based out ofRedwood City, CA on a hybrid basis.

Essential Duties and Responsibilities will include:

The Sr. Director, US Compliance will collaborate and build strong partnerships with several cross-functional stakeholders to help enable commercialization and growth within the NSCLC space. Areas of focus include:
  • Serve as the strategic compliance advisor to Commercial, Medical Affairs, Market Access, Patient Services, and other field-facing functions by proactively identifying compliance risks, enabling compliant business solutions, and embedding compliance into key business decisions throughout commercialization and product launch.
  • Lead ongoing compliance risk assessments for field-facing activities in the NSCLC space, identify emerging risks, and develop practical mitigation strategies in partnership with business leaders and others in Compliance.
  • Represent Compliance on commercialization committees, launch teams and workstreams, and other strategic and tactical decision-making forums, ensuring compliance considerations are incorporated into strategic business decisions.
  • Serve as lead compliance reviewer and advisor on NSCLC initiatives, ensuring timely, practical, and risk-based guidance is incorporated into business activities.
  • Lead the design, development, and delivery of engaging, risk-based compliance training to NSCLC business teams, ensuring compliance risks are appropriately mitigated while fostering a culture of ethics and compliance.
  • Partner with others in Compliance and business stakeholders to develop and continuously improve compliance policies, processes, and other governance controls.
  • Develop, manage, and conduct monitoring and auditing activities to identify and mitigate compliance risks.
  • Champion a culture of ethics, integrity, and accountability by promoting open communication, encouraging appropriate escalation of concerns, and reinforcing ethical decision-making.
  • Serve as strategic advisor in continuously improving the Compliance program by proposing enhancements, monitoring industry trends and best practices, and bringing the field perspective to discussions.
  • When appropriate given the business growth, build a team of compliance professionals to support the growing NSCLC commercialization field activities.
  • Partner closely with the Healthcare Law team to ensure consistency between legal interpretation and compliance operations.

Additional Responsibilities and Role Evolution

The responsibilities outlined in this job description are intended to describe the general nature and level of work performed by the individual in this role and are not intended to be an exhaustive list of all duties, responsibilities, or qualifications.

The Sr. Director, US Compliance will be expected to take on additional assignments, projects, and responsibilities as needed to support the Compliance team and broader business objectives. Responsibilities may change, expand, or shift over time based on organizational priorities, business growth, process improvements, technology implementations, and evolving legal or regulatory requirements.

The successful candidate will demonstrate flexibility, adaptability, and a willingness to contribute beyond the core responsibilities of the position, partnering collaboratively across functions to support the continued success and growth of the company.

Required Skills, Experience and Education:
  • Bachelor's degree.
  • 10+ years of healthcare compliance experience in pharmaceuticals or biotechnology; in-house compliance experience strongly preferred.
  • In-depth understanding of US healthcare laws and guidance, including the OIG guidelines, PhRMA Code, US Sunshine Law, Anti-Kickback Statute, False Claims Act, FDA promotional regulations, and the FCPA.
  • Experience as a compliance business partner with familiarity with the compliance risks associated with relevant business activities.
  • Significant experience supporting pre-commercial pharma or biotech companies through launch planning and commercial product launch.
  • 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.
  • Demonstrated experience leading, developing, and mentoring compliance professionals, or successfully leading through influence in a matrixed organization.
  • Experience leveraging data, insights, and compliance metrics to identify trends and prioritize risk mitigation activities.
  • 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.
  • Ability to travel as required (approximately 25%).

#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

$244,000-$305,000 USD

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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