Therapeutic Area Head of Regulatory Affairs

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profile Job Location:

Redwood City, CA - USA

profile Monthly Salary: Not Disclosed
Posted on: Yesterday
Vacancies: 1 Vacancy

Job Summary

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The companys 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 Revolutionariesin a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

The Opportunity:

  • Provide management and leadership of one or more therapeutic areas for late-stage oncology programs.

  • Oversee the development of global regulatory therapeutic area and product strategies to drive product development global registration and effective regulatory agency interactions.

  • Provide regulatory expertise and guidance to therapeutic area commercialization teams and other governance bodies.

  • Foster the career development of staff within the therapeutic area and contribute to departmental leadership activities.

  • Ensure alignment and consistency across programs within a therapeutic area based on regulatory intel research and competitive landscape.

Primary Responsibilities:

  • Direct the development of global regulatory strategy from registrational studies to marketing application across one or more therapeutic areas.

  • Lead and mentor GRLs/Study Leads in the development of global regulatory strategies in partnership with regional regulatory leads including precedence risk management and contingency planning.

  • Partner with regional regulatory leads to incorporate regional regulatory scientific clinical and market insights into integrated disease area and product strategies.

  • Communicate to management aligned global regulatory strategy and plans for a therapeutic area to support portfolio and life cycle management.

  • Conduct management review and approval of key documents for regulatory submissions and governance communications.

  • Contribute to the target product profile and evaluation of probability of regulatory success.

  • Monitor assess and communicate to staff impact of relevant global regulations guidance and current regulatory environment.

  • Advise on global health authority interactions and participate on core regulatory and cross-functional teams to ensure effective agency interactions.

  • Provide managerial leadership & direction to staff within the therapeutic area allowing appropriate prioritization of resources to achieve corporate goals.

  • Provide coaching mentoring and development of staff ensuring staff are compliant with Revolution Medicines corporate and departmental policies and procedures.

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.

  • Prior marketing application filing experience. Demonstrated success in obtaining health authority approvals.

  • Demonstrated ability in leading teams establishing organizational direction and championing continuous improvements.

  • Direct experience with global oncology drug development.

  • Experienced in representing Regulatory on cross functional teams and presenting to senior management. Proven ability to anticipate challenges and future risks and mitigate against potential strategic issues.

  • Excellent planning and organizational skills and the ability to work simultaneously on multiple projects with tight timelines.

Preferred Skills:

  • An advanced degree is desirable.

  • Experience with combination studies multiple expansion cohort global registrational studies basket or umbrella and master protocols highly preferred.

    #LI-Hybrid #LI-SH1

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.

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 ourCCPA additional information please contact.

Base Pay Salary Range
$244000$305000 USD

Required Experience:

Director

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The companys R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins and RAS Compa...
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