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Revolution Medicines

Clinical-stage oncology company developing RAS inhibitors

Senior Director - US Compliance

Full-Time
$244k - $305k+ Equity awards
Expert
Bachelor's
Redwood City, CA, USA
HybridHybrid work arrangement; approximately 25% travel required.
Risk & ComplianceRegulatory Compliance & Ethics

About the job

Requirements
  • A bachelor's degree is required.
  • At least 10 years of healthcare compliance experience in pharmaceuticals or biotechnology is required; in-house compliance experience is strongly preferred.
  • In-depth understanding of United States healthcare laws and guidance, including the Office of Inspector General guidelines, PhRMA Code, United States Sunshine Law, Anti-Kickback Statute, False Claims Act, Food and Drug Administration promotional regulations, and Foreign Corrupt Practices Act.
  • Experience as a compliance business partner and familiarity with compliance risks associated with relevant business activities.
  • Significant experience supporting pre-commercial pharmaceutical or biotechnology companies through launch planning and commercial product launch.
  • Ability to build strong partnerships and collaborate with internal and external partners at all organizational levels.
  • Strategic and pragmatic compliance mindset with strong business acumen.
  • High ethical standards, sound judgment, and commitment to fostering integrity, transparency, and continuous improvement.
  • Leadership, communication, analytical, and problem-solving skills, and ability to collaborate with legal, scientific, and business functions.
  • Demonstrated experience leading, developing, and mentoring compliance professionals, or successfully leading through influence in a matrixed organization.
  • Experience using data, insights, and compliance metrics to identify trends and prioritize risk mitigation activities.
  • Presentation, organizational, and project management skills, including ability to handle multiple high-priority projects simultaneously.
  • Ability to travel as required, approximately 25%.
Responsibilities
  • 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 non-small cell lung cancer space, identify emerging risks, and develop practical mitigation strategies with business leaders and others in Compliance.
  • Represent Compliance on commercialization committees, launch teams, 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 non-small cell lung cancer 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 non-small cell lung cancer business teams, mitigating compliance risks while fostering a culture of ethics and compliance.
  • Partner with Compliance colleagues 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.
  • Promote open communication, encourage appropriate escalation of concerns, and reinforce ethical decision-making to champion a culture of ethics, integrity, and accountability.
  • Propose enhancements to the Compliance program, monitor industry trends and best practices, and bring the field perspective to discussions.
  • When appropriate as the business grows, build a team of compliance professionals to support growing non-small cell lung cancer commercialization field activities.
  • Partner closely with the Healthcare Law team to ensure consistency between legal interpretation and compliance operations.
  • Take on additional assignments, projects, and responsibilities as needed to support the Compliance team and broader business objectives; responsibilities may change, expand, or shift with organizational priorities, business growth, process improvements, technology implementations, and evolving legal or regulatory requirements.
Desired Qualifications
  • In-house compliance experience is strongly preferred.

About the company

Revolution Medicines develops targeted therapies for cancers caused by RAS mutations, which are found in about 30% of human cancers. The company’s products are small molecules called RAS(ON) inhibitors that work by blocking the active, cancer-promoting form of the RAS protein to stop tumor growth. Unlike older treatments that could only target a few specific mutations, this platform creates inhibitors that can address a much wider range of RAS-driven cancers. The company's goal is to advance these candidates through clinical trials to provide effective treatment options for patients with previously "undruggable" forms of cancer.

Company Size

1,001-5,000

Company Stage

IPO

Headquarters

Redwood City, California

Founded

2014

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Simplify's Take

What believers are saying

  • FDA approved RASONQUE on August 26, 2026, six months ahead of deadline.
  • RASolute 302 cut death risk 60% and doubled median overall survival to 13.2 months.
  • Royalty Pharma's June 2025 $2 billion package funds commercialization and global expansion through 2027.

What critics are saying

  • RASONQUE costs $39,800 monthly, inviting Medicare and commercial payer restrictions in 2026.
  • Revenue still depends overwhelmingly on one launch; any RASONQUE setback crushes the company.
  • AstraZeneca, Amgen, and Mirati pressure RAS programs; resistance or safety issues can erase the franchise.

What makes Revolution Medicines unique

  • RASONQUE became the first approved broad RAS(ON) inhibitor on August 26, 2026.
  • Revolution Medicines avoids companion diagnostics and treats metastatic PDAC with or without RAS mutations.
  • Its pipeline spans daraxonrasib, elironrasib, and zoldonrasib across pancreatic, lung, and colorectal cancers.

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Benefits

Company Equity

Growth & Insights and Company News

Headcount

6 month growth

-1%

1 year growth

-2%

2 year growth

-1%
Kalkine
Oct 13th, 2026
Revolution Medicines draws $250M Royalty Pharma loan after FDA approval, declines royalty tranche

Revolution Medicines has drawn a $250 million term loan from Royalty Pharma Development Funding, LLC after the US Food and Drug Administration (FDA) approved its pancreatic cancer drug RASONQUE (daraxonrasib). The company disclosed the October 8, 2026 draw in a Form 8-K filed October 13. The loan carries interest at three-month Term SOFR, with a 3.50% floor, plus 5.75%. It is interest-only, with principal due October 8, 2032. Revolution Medicines paid a $5 million draw fee. The company declined a separate royalty option under which Royalty Pharma Investments 2019 ICAV would have paid up to $250 million. The loan is the first tranche of a facility of up to $750 million, agreed on June 23, 2025. Up to $500 million in further loans remains potentially available, subject to milestones and conditions.

Gizmodo
Sep 30th, 2026
This pill will change cancer treatment forever.

This pill will change cancer treatment forever. Revolution Medicines' daraxonrasib is the first drug that can broadly tackle one of the main drivers of pancreatic cancer. By Ed Cara Published September 30, 2026, 7:08 am ET Reading time 4 minutes Revolution Medicines is the winner of the 2026 Gizmodo Science Fair for its research and development of Rasonque (daraxonrasib), the first approved cancer drug of its kind. The question. Can we find an effective and reliable treatment for pancreatic cancer, which currently only has a five-year survival rate of 13%? The results. In a large-scale clinical trial of 500 people with metastatic pancreatic ductal adenocarcinoma (the most common form of pancreatic cancer), people on daraxonrasib lived twice as long as those on standard chemotherapy: 13.2 months median survival compared to 6.7 months. The treatment group also lived longer without progression of their cancer, and the drug was relatively well-tolerated, with only about 1% discontinuing the drug. In late August, the Food and Drug Administration approved Rasonque for people with pancreatic ductal adenocarcinoma who have already tried at least one prior systemic therapy or who are not candidates for multiagent systemic therapy. Why they did it. RevMed originally began in 2014 as a natural product chemistry company focused on finding novel treatments for infections, according to Jan Smith, RevMed's chief scientific officer. After its early efforts failed to take off, however, the company made a pivotal decision to move into oncology, Smith said, "recognizing that cancer represented one of the most meaningful opportunities to make a difference for patients." Like many scientific discoveries, RevMed researchers didn't purposefully set out to develop drugs like daraxonrasib. They began working on a drug candidate designed to inhibit SHP2, an enzyme that transmits growth signals from outside a cancer cell to a pathway inside the cell governed by RAS, a family of proteins that many in the field had considered impossible to directly target with drugs. To their surprise, their candidate could actually shrink tumors fueled by mutations of RAS, something that wasn't supposed to happen. "This observation led us to the realization that we had 'a tiger by the tail' and needed to go after RAS itself," Smith said. "Despite RAS being the first genetic driver of human cancer ever discovered, RAS-driven cancers have defied targeted treatment approaches for decades, making RAS truly the holy grail target of oncology." Daraxonrasib is specifically the first approved medication in a class of drugs known as RAS(ON) inhibitors. RAS acts as a sort of switch for cell growth, and cancer-fueling RAS mutations force the protein to be stuck in its active "ON" state, driving further growth. Daraxonrasib and similar agents bind to and block activity from mutant RAS proteins left in this state. "These inhibitors harness a naturally occurring protein in cells to create a complex with a precisely engineered, large surface area that establishes a molecular foothold on the smooth, featureless surface of RAS(ON), enabling direct inhibition of RAS in its oncogenic state," explained Smith. Why they're a winner. It's hard to oversell just how earthshaking RevMed's breakthrough is. Scientists have made great strides in treating many different kinds of cancer, with the notable exception of pancreatic cancer. We're even less equipped to handle metastatic pancreatic cancer, which currently has a five-year survival rate of 3%. However, the vast majority of pancreatic cancers, around 90%, are fueled by RAS mutations. And though daraxonrasib isn't the first approved drug that targets RAS, it is the first that attacks a broad range of RAS mutations, which should allow it to target much of that 90% slice. Right now, the drug is only meant for cases that haven't responded to other treatments, but RevMed has already launched a phase III trial testing it as a frontline drug for metastatic pancreatic ductal adenocarcinoma. To be clear, daraxonrasib is not a cure. Some people don't respond to the drug initially, and even when they do, their cancers can often still adapt to the treatment over time and find ways to keep growing. But daraxonrasib will give doctors and patients the first real fighting chance they've had against pancreatic cancer, and it's likely only the start of a new era. What's next. RevMed has eight phase III trials that it has either completed, is actively carrying out, or plans to launch by the end of 2026, and its researchers are working to deepen their pipeline. Though daraxonrasib is a broad-reaching inhibitor, the company is also developing other candidates that more narrowly go after specific RAS mutations. "We're progressing both multi- and mutant-selective approaches to explore new potential treatment options for RAS-driven cancers," Smith said. Further down the line, the company is hoping to pioneer drugs that can counteract a cancer's resistance to RAS-targeted therapies. Notably, pancreatic cancer isn't the only type often driven by RAS mutations; up to 50% of colorectal cancers involve these mutations, as do around a third of lung adenocarcinomas. Several of the company's trials are testing drugs for non-small cell lung cancers as well as solid tumors associated with RAS. The team. It's taken plenty of resources and teamwork for RevMed to reach the top of the mountain. One critical aspect of its success was the acquisition of the company Warp Drive Bio in 2018, which pioneered the tri-complex inhibitor platform that eventually made daraxonrasib a reality. "This research has required collaboration across multiple disciplines and organizations. Our internal team spans deep expertise in chemical biology, cancer biology, structure-based and computationally assisted drug discovery, medicinal chemistry, pharmacology, translational research and clinical oncology," Smith said. And of course, none of this would be possible without the many cancer patients who volunteered their time and bodies. As of now, the company has treated more than 2,500 people with one or more of its RAS(ON) inhibitors. And because of them, the roughly 67,000 Americans diagnosed annually with pancreatic cancer now have more hope than ever.

Yahoo Finance
Sep 11th, 2026
Revolution Medicines' first pancreatic cancer therapy approval challenges Amgen's biotech dominance

Revolution Medicines received FDA approval for daraxonrasib, the first targeted therapy for metastatic pancreatic cancer, after clinical data showed it reduced death risk by more than half. The company is clinical-stage with no current revenue and posted a $1.1 billion net loss in FY 2025. Amgen reported FY 2025 revenue of $36.7 billion, up 9.9% year-over-year, with net income of $7.7 billion and a 21% net margin. Free cash flow reached $8.1 billion. The company carries a debt-to-equity ratio of 6.3x. Revolution Medicines maintains a 0.1x debt-to-equity ratio and 9.5x current ratio but recorded negative free cash flow of $913.7 million. The company's pipeline targets RAS-driven tumours including lung cancer. A partnership with Royalty Pharma provides funding for development. Both companies face distinct risks: Amgen confronts pricing pressures and biosimilar competition, whilst Revolution Medicines carries clinical trial failure risks and competes against larger pharmaceutical firms.

Yahoo Finance
Aug 29th, 2026
Revolution Medicines wins FDA approval for first RAS-targeted pancreatic cancer drug

The US Food and Drug Administration approved Rasonque (daraxonrasib), a once-daily pill from Revolution Medicines, for adults with metastatic pancreatic cancer who have had chemotherapy. It is the first broad RAS-targeted medicine cleared for this indication. Most pancreatic tumours are driven by mutated RAS protein, present in over 90% of cases. In the Phase 3 trial of 500 patients, Rasonque nearly doubled median overall survival to 13.2 months, up from 6.7 months on standard chemotherapy. The FDA cleared the drug about 35 days after accepting the application, using the Commissioner's National Priority Voucher programme. Over 2,000 patients had already received Rasonque through an expanded access programme before full approval.

Yahoo Finance
Aug 28th, 2026
Revolution Medicines wins FDA approval in one month, analysts project $11.5B peak sales for pancreatic cancer drug

Revolution Medicines secured FDA approval for its pancreatic cancer drug daraxonrasib just one month after filing, through the agency's expedited Commissioner's National Priority Voucher programme. The drug, branded Rasonque, treats metastatic pancreatic cancer in adults who have received prior systemic therapy or are ineligible for combination treatment. Rasonque works by blocking several forms of the RAS protein using a novel "molecular glue" mechanism. Phase 3 data presented in April showed statistically significant improvements across all primary and secondary endpoints compared with traditional chemotherapy. Analysts project peak sales of $11.5 billion for the treatment. The approval prompted significant investor attention and a substantial share price increase for the biotech company.