Backed by GV.
About the role
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. Provide support for the preparation, quality review, and coordination of regulatory submission documents and global CTA submissions across programs.
What they're looking for
- 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 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
- Experience in oncology drug development
More about this role
Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide.
Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor—all in service of patients.
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.
Provide support for the preparation, quality review, and coordination of regulatory submission documents and global CTA submissions across programs.
Establish and manage the Regulatory...
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