revolutionmedicines
Senior Safety Scientist II
At a Glance
- Location
- Redwood City, California, United States
- Work Regime
- hybrid
- Experience
- 3+ years
- Posted
- 2026-07-17T14:24:27-04:00
Key Requirements
Required Skills
Domain Knowledge
- Clinical
- Education
- Energy
- Finance
- Medical
- Pharmaceutical
Requirements
5 or more years of drug development experience in the pharmaceutical or related industry with at least 3 years in drug safety.
Proven success in creating and sustaining strong relationships with internal and external business partners across an organization to create positive partnerships.
Broad understanding of the scientific aspects of safety, PV (including GVP, GCP), and clinical/patient risk management and safety operations.
Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high-energy environment.
Strong organizational skills and an ability to interpret, discuss, and report trial level data effectively and identify trends.
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.
Compensation & Benefits
$186,000
—
$233,000 USD
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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. All legitimate communication from Revolution Medicines will come from an official
@revmed.com
Responsibilities
The Senior Safety Scientist within Global Patient Safety Science is an individual contributor who provides safety science and pharmacovigilance support to all products across the RevMed portfolio, which includes early and late phase development activities.
The individual will be responsible for safety oversight of clinical studies, review and authoring of clinical trial protocols, IBs, ICFs, and DSURs.
Additional safety related activities will involve medical review of individual case safety reports (ICSRs), safety surveillance of assigned products and active member of cross-functional teams.
The Senior Safety Scientist will develop and maintain an understanding of the safety profile of the assigned product(s).
Proactive medical safety surveillance of ongoing clinical trials for identification and management of safety signals.
Prepare and present safety data summaries to internal and external stakeholders.