Senior Associate, Regulatory Affairs

1 week ago


Redwood City, United States REVOLUTION Medicines Full time

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.

The Opportunity:

The Senior Associate Regulatory Affairs will support Senior Regulatory Affairs management in day-to-day operational aspect of the department and will support interactions with global regulatory authorities.

  • Represent Regulatory Affairs on project teams and closely collaborate with multidisciplinary teams to identify submission requirements, coordinate the content and development process (planning, creation, review, and approval) of selected regulatory documentation for inclusion in submissions to global health authorities.
  • Compile regulatory submissions that meet ICH or FDA requirements, other local or regional regulatory requirements, as applicable, and company policies and procedures.
  • Prepare and manage routine submissions and related activities. Define and manage detailed timelines to ensure timely delivery of high-quality, compliant, accurate and complete regulatory submissions.
  • Assist in the development and implementation of SOPs and systems to track and manage product-associated events.
  • Investigate and evaluate regulatory history/background of class, disease/therapeutic/diagnostic context to assist in assessment of regulatory implications for development and approval. Assist in the development of regulatory strategy and update strategy based upon regulatory changes.
  • Stay abreast of changes in the regulatory environment and guidelines (e.g., FDA, ICH) in areas relevant to company projects.
  • Work with manager on acquisition and development of required regulatory skills and knowledge.
Required Skills, Experience and Education:
  • Bachelor's degree in a relevant field.
  • Two or more years prior experience in a Regulatory Affairs department at a drug or biologics company.
  • Some familiarity with regulatory requirements for development of drug and biological products, including FDA regulations and guidance, and ICH guidelines.
  • Willing to advance my knowledge of regulatory practice through classes, certifications, webinars.
  • Technical expertise with Windows, MS Office (Outlook, Word, Excel), Adobe Acrobat software systems, and experience working in an electronic document management system.
Preferred Skills:
  • Experience in oncology drug development
  • Experience with supporting the preparation and submission of large complex regulatory submissions, including NDA's
  • Excellent written and verbal communication skills

The base salary range for this full-time position is $95,000 to $120,000 for candidates based at our headquarters in Redwood City, CA. The range displayed on each job posting is intended to be the minimum and maximum salary for the position in Redwood City and will be adjusted for the local market a candidate is based. 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.

#LI-Hybrid #LI-JC1

  • Redwood City, United States Planet Pharma Full time

    The Opportunity:The Senior Associate Regulatory Affairs will support Senior Regulatory Affairs management in day-to-day operational aspect of the department and will support interactions with global regulatory authorities.Represent Regulatory Affairs on project teams and closely collaborate with multidisciplinary teams to identify submission requirements,...


  • Redwood City, California, United States Revolution Medicines Full time

    Job Summary:Revolution Medicines is seeking a Senior Manager, Regulatory Affairs to provide regulatory advice and guidance to project teams.Key Responsibilities:Manage and coordinate Regulatory Affairs activities within and between departments.Obtain and maintain National Health Authority approvals for investigational products.Manage planning, preparation,...


  • Redwood City, United States REVOLUTION Medicines Full time

    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...


  • redwood city, United States Planet Pharma Full time

    The Opportunity:The Senior Associate Regulatory Affairs will support Senior Regulatory Affairs management in day-to-day operational aspect of the department and will support interactions with global regulatory authorities.Represent Regulatory Affairs on project teams and closely collaborate with multidisciplinary teams to identify submission requirements,...


  • Redwood City, CA, United States Adverum Biotechnologies Full time

    The Talent Acquisition / HR team manages the recruiting for all positions at Adverum. We only accept resumes from search agencies or recruiters if the Talent Acquisition / HR team has formally requested your help and have a signed agreement in place. Unsolicited resumes sent to Adverum will be considered property of Adverum. The company will not be...


  • redwood city, United States Nuvig Therapeutics Inc. Full time

    Why Nuvig Be a part of a potential game-changer for patients with autoimmune disease! Nuvig Therapeutics is developing novel immune therapies to treat a broad spectrum of autoimmune diseases. Our treatments are developed to be active for a broad spectrum of autoimmune diseases, without the inherent side effects and safety concerns of long-term treatment with...


  • redwood city, United States Nuvig Therapeutics Inc. Full time

    Why Nuvig Be a part of a potential game-changer for patients with autoimmune disease! Nuvig Therapeutics is developing novel immune therapies to treat a broad spectrum of autoimmune diseases. Our treatments are developed to be active for a broad spectrum of autoimmune diseases, without the inherent side effects and safety concerns of long-term treatment with...


  • Redwood City, United States Nuvig Therapeutics Inc. Full time

    Why Nuvig Be a part of a potential game-changer for patients with autoimmune disease! Nuvig Therapeutics is developing novel immune therapies to treat a broad spectrum of autoimmune diseases. Our treatments are developed to be active for a broad spectrum of autoimmune diseases, without the inherent side effects and safety concerns of long-term treatment with...


  • Redwood City, United States Work In Biotech Full time

    Why Nuvig Be a part of a potential game-changer for patients with autoimmune disease!  Nuvig Therapeutics is developing novel immune therapies to treat a broad spectrum of autoimmune diseases.  Our treatments are developed to be active for a broad spectrum of autoimmune diseases, without the inherent side effects and safety concerns of long-term treatment...


  • Foster City, United States ATR International Full time

    Job DescriptionJob DescriptionWe are seeking a Senior Manager, Regulatory Affairs III for a very important client. RESPONSIBILITIES MAY INCLUDE• Responsible for preparation of the Quality sections of INDs/IMPDs, new marketing authorization applications, post-approval variations, renewals and responses to agency questions, for a range of biologics...


  • Foster City, United States ATR International Full time

    Job DescriptionJob DescriptionWe are seeking a Regulatory Affairs Assistant - II for a very important client. Specific Job Responsibilities• Perform data entry using Gilead RIM System to enter relevant information to support key CMC RA stakeholders.• Work collaboratively to support the team by executing routine data entry, such as the input of...


  • Foster City, California, United States ATR International Full time

    Job Title: Regulatory Affairs Manager - Biologics ExpertAbout the Role:We are seeking a highly experienced Senior Manager, Regulatory Affairs III to join our team at ATR International.Job Description:Key Responsibilities:Preparation of quality sections for INDs/IMPDs, new marketing authorization applications, post-approval variations, renewals, and responses...


  • new york city, United States Arevna Full time

    Director of Regulatory Affairs and Compliance - Women’s HealthLocation: New JerseyWe’re seeking an experienced Director of Regulatory Affairs and Compliance to join a leading women’s health-focused organization based in New Jersey. In this role, you’ll drive regulatory strategies and compliance initiatives to support FDA approvals and maintain...


  • new york city, United States Arevna Full time

    Director of Regulatory Affairs and Compliance - Women’s HealthLocation: New JerseyWe’re seeking an experienced Director of Regulatory Affairs and Compliance to join a leading women’s health-focused organization based in New Jersey. In this role, you’ll drive regulatory strategies and compliance initiatives to support FDA approvals and maintain...


  • Jersey City, New Jersey, United States Hays Recruitment Full time

    Job Summary:We are seeking a highly motivated and experienced Regulatory Affairs Specialist to join our team. In this role, you will be responsible for assisting the Regulatory Team with maintenance and registration of new products and state wholesaler licenses as required by regulatory agencies.About the Role:Provide regulatory support to all functional...


  • Salt Lake City, United States ARUP Laboratories Full time

    Description Schedule :Monday - Friday (40 hrs/wk)8:00 AM - 5:00 PM Department: Corp Compliance Office - 241 Primary Purpose : The Regulatory Affairs Coordinator is a member of the Corporate Compliance office and supports the Public Health Reporting team and Compliance Manager. The Regulatory Affairs Coordinator ensures compliance to new and existing...


  • Salt Lake City, United States Menlo Ventures Full time

    Your work will change lives. Including your own. The Impact You’ll Make Recursion is at the forefront of reimagining drug discovery and development through broadening the funnel of potential targets, using technology and standardization to build connected data, and superlinearly scaling our efforts to accelerate the delivery of high-potential drug...


  • Salt Lake City, United States Menlo Ventures Full time

    Your work will change lives. Including your own. The Impact You’ll Make Recursion is at the forefront of reimagining drug discovery and development through broadening the funnel of potential targets, using technology and standardization to build connected data, and superlinearly scaling our efforts to accelerate the delivery of high-potential drug...


  • Oklahoma City, Oklahoma, United States Urban Affairs Association Full time

    About Urban Affairs AssociationAt the Urban Affairs Association, we are committed to addressing real property issues that impact disadvantaged communities. Our team is dedicated to developing legal reform and policy proposals to address critical land and housing issues at the local, state, and federal level.


  • Jersey City, New Jersey, United States Hays Recruitment Full time

    Job SummaryIn this role, you will assist the Regulatory Team with maintenance and registration of new products and state wholesaler licenses as required from the FDA and other regulatory agencies.Key Responsibilities:Provide regulatory support to all functional groups.Submit electronic documentation through the Electronic Submissions Gateway (ESG).Create,...