Revolution Medicines
Director, Regulatory Affairs
Revolution Medicines, San Francisco, California, United States, 94199
Join to apply for the
Director, Regulatory Affairs
role at
Revolution Medicines 2 days ago Be among the first 25 applicants Join to apply for the
Director, Regulatory Affairs
role at
Revolution Medicines Get AI-powered advice on this job and more exclusive features. Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.
Make sure to apply with all the requested information, as laid out in the job overview below.
The Opportunity:
The Director of Regulatory Affairs is accountable for the delivery of regulatory strategy for designated programs at RevMed. They will support programs and drug development teams and ensure delivery of targeted, pragmatic, well-vetted, consistent and actionable regulatory advice. The Director will support policy and process development within regulatory and cross-functionally to define a consistent RevMed approach to regulatory advice and strategy. The Director must have a thorough understanding of and be highly experienced in oncology drug development, applicable regulations, and current health authority thinking, and have strong leadership and relationship-building ability.
Provide clear, effective regulatory strategy as the Regulatory Study Lead for global oncology programs. Motivate, mentor and develop direct reports to ensure development and performance. Ensure late-stage oncology programs are fully resourced and anticipate regulatory needs to deliver on program milestones. Develop robust global regulatory strategies that reflect competitive intelligence, expert input, and align with corporate goals to ensure global success. Drive consistency in regulatory approach, ensuring lessons learned across programs are applied broadly. Establish highly collaborative and effective relationships with management colleagues in Clinical Research, Clinical Operations, Regulatory Affairs, Medical Writing, Quality and other functions to ensure cross-functional alignment and team effectiveness.
Required Skills, Experience and Education:
Degree in life sciences, pharmacy, medicine, or related fields with a minimum of 12 years in the pharmaceutical/biotech industry or relevant work experience and a minimum of 8 years in Regulatory Affairs including regulatory strategy and leadership roles. Proven success in developing and delivering global regulatory strategies and submissions. Demonstrated success in leading health authority interactions and negotiations. Direct experience in oncology drug development including oversight of large, global Phase 3 studies. Skilled at representing Regulatory on cross-functional teams and presenting to senior leadership. Excellent communication, planning, and organizational skills with the ability to manage multiple projects and tight deadlines.
Preferred Skills:
An advanced degree is desirable. Experience with dose optimization in oncology. Prior NDA experience is highly preferred.
The base salary range for this full-time position is $204,000 to $255,000 for candidates working onsite at our headquarters in Redwood City, CA. The range displayed on each job posting is intended to be the salary for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our salary ranges are determined by role, level, and location. Individual pay is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.
Please note that base salary 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.
Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.
Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy . For additional information, please contact privacy@revmed.com .
Seniority level
Seniority levelNot Applicable Employment type
Employment typeFull-time Job function
Job functionLegal Referrals increase your chances of interviewing at Revolution Medicines by 2x Get notified about new Director of Regulatory Affairs jobs in
San Francisco Bay Area . Director, Regulatory Affairs - Job ID: DRAVice President / Head of Regulatory AffairsDirector / Senior Director, Regulatory AffairsSenior Director, Regulatory Affairs - Job ID: 1668Associate Director/ Director Regulatory Affairs CMC Foster City, CA $191,250.00-$272,250.00 2 weeks ago Global Head of Quality and Regulatory Affairs, Lingo Alameda, CA $193,300.00-$386,700.00 2 weeks ago Associate Director, Regulatory Affairs - Global Labeling Foster City, CA $165,495.00-$235,620.00 1 week ago Associate Director of Regulatory AffairsAssociate Director Regulatory Affairs – APAC - Diabetes Care Alameda, CA $146,700.00-$293,300.00 5 months ago Director, CMC Regulatory Affairs – BiologicsSenior Manager, Global Regulatory Strategy US & Canada (Hybrid Onsite) San Francisco, CA $121,000.00-$230,000.00 2 weeks ago San Francisco, CA $182,000.00-$227,100.00 2 weeks ago Director, Corporate Quality Management Systems Santa Cruz, CA $165,607.89-$248,411.84 1 month ago Associate Vice President of Diagnostics Regulatory Affairs Santa Clara, CA $175,440.00-$328,950.00 6 days ago Sunnyvale, CA $143,400.00-$197,100.00 6 days ago Commercial Regulatory Affairs Director (Advertising and Promotion) Alameda, CA $167,500.00-$237,500.00 1 week ago Senior Manager, Global Regulatory Strategy US & Canada (Hybrid Onsite) San Francisco, CA $121,000.00-$230,000.00 3 hours ago Sunnyvale, CA $143,400.00-$197,100.00 6 days ago Director Life Sciences Regulatory Affairs and Labeling South San Francisco, CA $180,000.00-$225,000.00 2 months ago Senior Director, GCP/GVP Quality Assurance San Francisco, CA $260,000.00-$275,000.00 5 days ago Fairfield, CA $180,252.50-$243,340.88 2 weeks ago South San Francisco, CA $190,000.00-$240,000.00 3 weeks ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr
Director, Regulatory Affairs
role at
Revolution Medicines 2 days ago Be among the first 25 applicants Join to apply for the
Director, Regulatory Affairs
role at
Revolution Medicines Get AI-powered advice on this job and more exclusive features. Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.
Make sure to apply with all the requested information, as laid out in the job overview below.
The Opportunity:
The Director of Regulatory Affairs is accountable for the delivery of regulatory strategy for designated programs at RevMed. They will support programs and drug development teams and ensure delivery of targeted, pragmatic, well-vetted, consistent and actionable regulatory advice. The Director will support policy and process development within regulatory and cross-functionally to define a consistent RevMed approach to regulatory advice and strategy. The Director must have a thorough understanding of and be highly experienced in oncology drug development, applicable regulations, and current health authority thinking, and have strong leadership and relationship-building ability.
Provide clear, effective regulatory strategy as the Regulatory Study Lead for global oncology programs. Motivate, mentor and develop direct reports to ensure development and performance. Ensure late-stage oncology programs are fully resourced and anticipate regulatory needs to deliver on program milestones. Develop robust global regulatory strategies that reflect competitive intelligence, expert input, and align with corporate goals to ensure global success. Drive consistency in regulatory approach, ensuring lessons learned across programs are applied broadly. Establish highly collaborative and effective relationships with management colleagues in Clinical Research, Clinical Operations, Regulatory Affairs, Medical Writing, Quality and other functions to ensure cross-functional alignment and team effectiveness.
Required Skills, Experience and Education:
Degree in life sciences, pharmacy, medicine, or related fields with a minimum of 12 years in the pharmaceutical/biotech industry or relevant work experience and a minimum of 8 years in Regulatory Affairs including regulatory strategy and leadership roles. Proven success in developing and delivering global regulatory strategies and submissions. Demonstrated success in leading health authority interactions and negotiations. Direct experience in oncology drug development including oversight of large, global Phase 3 studies. Skilled at representing Regulatory on cross-functional teams and presenting to senior leadership. Excellent communication, planning, and organizational skills with the ability to manage multiple projects and tight deadlines.
Preferred Skills:
An advanced degree is desirable. Experience with dose optimization in oncology. Prior NDA experience is highly preferred.
The base salary range for this full-time position is $204,000 to $255,000 for candidates working onsite at our headquarters in Redwood City, CA. The range displayed on each job posting is intended to be the salary for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our salary ranges are determined by role, level, and location. Individual pay is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.
Please note that base salary 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.
Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.
Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy . For additional information, please contact privacy@revmed.com .
Seniority level
Seniority levelNot Applicable Employment type
Employment typeFull-time Job function
Job functionLegal Referrals increase your chances of interviewing at Revolution Medicines by 2x Get notified about new Director of Regulatory Affairs jobs in
San Francisco Bay Area . Director, Regulatory Affairs - Job ID: DRAVice President / Head of Regulatory AffairsDirector / Senior Director, Regulatory AffairsSenior Director, Regulatory Affairs - Job ID: 1668Associate Director/ Director Regulatory Affairs CMC Foster City, CA $191,250.00-$272,250.00 2 weeks ago Global Head of Quality and Regulatory Affairs, Lingo Alameda, CA $193,300.00-$386,700.00 2 weeks ago Associate Director, Regulatory Affairs - Global Labeling Foster City, CA $165,495.00-$235,620.00 1 week ago Associate Director of Regulatory AffairsAssociate Director Regulatory Affairs – APAC - Diabetes Care Alameda, CA $146,700.00-$293,300.00 5 months ago Director, CMC Regulatory Affairs – BiologicsSenior Manager, Global Regulatory Strategy US & Canada (Hybrid Onsite) San Francisco, CA $121,000.00-$230,000.00 2 weeks ago San Francisco, CA $182,000.00-$227,100.00 2 weeks ago Director, Corporate Quality Management Systems Santa Cruz, CA $165,607.89-$248,411.84 1 month ago Associate Vice President of Diagnostics Regulatory Affairs Santa Clara, CA $175,440.00-$328,950.00 6 days ago Sunnyvale, CA $143,400.00-$197,100.00 6 days ago Commercial Regulatory Affairs Director (Advertising and Promotion) Alameda, CA $167,500.00-$237,500.00 1 week ago Senior Manager, Global Regulatory Strategy US & Canada (Hybrid Onsite) San Francisco, CA $121,000.00-$230,000.00 3 hours ago Sunnyvale, CA $143,400.00-$197,100.00 6 days ago Director Life Sciences Regulatory Affairs and Labeling South San Francisco, CA $180,000.00-$225,000.00 2 months ago Senior Director, GCP/GVP Quality Assurance San Francisco, CA $260,000.00-$275,000.00 5 days ago Fairfield, CA $180,252.50-$243,340.88 2 weeks ago South San Francisco, CA $190,000.00-$240,000.00 3 weeks ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr