Revolution Medicines
Associate Director, Regulatory Science
Remote (United States) · Director · Full-time
Stay score
odds of building a lasting career here
Sponsors, but it's cap-subject — you still face the weighted lottery (~61% per draw at Level IV). Good if you win; have a cap-exempt backup on your list.
Lottery odds assume a STEM candidate.
Personalize to your clock →Employer immigration record
from this employer's Department of Labor filings
Files H-1B transfers
Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.
Community outcomes
No reports yet — be the first to help the next applicant.
About the role
- The Associate Director of Regulatory Science may represent regulatory science on cross-functional teams and provide regulatory advice on clinical development matters.
- Plan, prepare, and coordinate regulatory submissions, ensuring high quality and timeline adherence.
- Able to proactively identify risks and devise mitigation strategies.
Responsibilities
- Develop, implement, and maintain initiatives, processes, and procedures with a recognition of when to consult departmental senior personnel concerning risks.
Requirements
- Bachelor's Degree in a relevant field, an advanced degree is desirable, with a minimum of 9+ years in the pharmaceutical/biotech industry or relevant work experience and a minimum of 5 years in Regulatory Affairs.
Nice to have
- Strong working knowledge of US FDA and EU EMA Pharmaceutical regulations and guidance.
- Experience with EU CTR submissions preferred.
Skills
- Experienced in representing Regulatory Science on cross functional teams and presenting to senior management. Excellent communicator.
- Excellent planning and organizational skills and the ability to work simultaneously on multiple projects with tight timelines.
- Strong working knowledge of US FDA and EU EMA Pharmaceutical regulations and guidance. Experience with EU CTR submissions preferred.
- Direct experience with oncology drug development highly preferred.
- Experience with combination studies, multiple expansion cohort, basket, or umbrella master protocols highly preferred.
- Direct experience with FDA expedited programs highly preferred.
- #LI-JC1 #LI-Remote
- The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below.
Compensation
- $177,000 - $221,000 USD
- Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process.
Benefits
- Experience in the preparation and submission of large, complex regulatory documentation to support health agency review/approval procedures, post approval activities.
Company info
- 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.
- Base Pay Salary Range $177,000 - $221,000 USD We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines.
- Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process.
This listing is sourced directly from Revolution Medicines's careers page and normalized into a canonical job model.