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Senior Associate, Regulatory Affairs

Revolution Medicines
Location
Redwood City, California, United States
Posted
17 days ago
Department
Regulatory Affairs
What they actually want (must-haves)
  • Bachelor’s degree in a relevant field
  • 4+ years' experience in a Regulatory Affairs department at a drug or biologics company
  • Familiarity with regulatory requirements for drug and biological products, including FDA regulations and ICH guidelines
  • Willingness to advance knowledge of regulatory practice through classes, certifications, webinars
  • Technical expertise with Windows, MS Office (Outlook, Word, Excel), Adobe Acrobat, and experience with electronic document management systems
Nice to have
  • 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
What the job really is

The Senior Associate in Regulatory Affairs at Revolution Medicines will support the management of the Regulatory Affairs department by facilitating interactions with global regulatory authorities. This role involves compiling regulatory submissions, managing timelines, and ensuring compliance with ICH and FDA requirements. Additionally, the associate will assist in developing regulatory strategies and stay updated on changes in the regulatory environment.

Benefits
  • Base pay salary range of $120,000 — $150,000 USD
  • Competitive cash compensation
  • Robust equity awards
  • Strong benefits
  • Significant learning and development opportunities
Things to weigh
  • No specific mention of remote work flexibility despite hybrid notation
  • Role may involve routine tasks alongside strategic responsibilities
  • Salary range provided but may vary based on multiple factors
Job score3/5
Benefits3/5
Freshness4/5
Career value4/5
Role clarity4/5
Pay transparency0/5

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