Senior Safety Scientist II

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins, including daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, currently in clinical development.

About the role

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, including 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 involve medical review of individual case safety reports (ICSRs), safety surveillance of assigned products, and active participation in cross-functional teams.

Responsibilities

• 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.
• Risk management activities, including medical review of ICSRs, routine review of safety data, and pertinent scientific literature articles.
• Acquire and contribute knowledge of relevant drug class and/or competitor safety issues.
• Identify potential clinical safety issues and recommend appropriate risk mitigation measures.
• Involvement in preparation and maintenance of relevant sections of clinical trial protocols, IBs (including the reference safety information section), ICFs, DSURs, RMPs, CCDS, and labelling, as required.
• Perform safety review of clinical protocols, Investigator's Brochure (IB), informed consent form (ICF), and other related documents to ensure alignment with the safety strategy and appropriateness of risk management strategies and risk communication.
• Accountable for the safety components of study reports (e.g., CSRs), publications, aggregate reports, and other regulatory documents.
• Conduct signal detection and evaluation activities for assigned products for continuous benefit-risk evaluation throughout the product lifecycle and contribute/lead preparation for escalation to safety governance committees.
• Support implementation of decisions from the signal evaluation process, including updates to core safety information, Investigator’s Brochure, and other key safety documents and deliverables.
• Contribute to input related to regulatory filings (e.g., New Drug Applications [NDAs], Biologics License Applications [BLAs]) and responses to safety queries from third parties, such as regulatory agencies.
• Establish and maintain collaborative working relationships with all key stakeholders (study team members, CROs, investigators, study sites, vendors, committees, etc.).
• Consistently comply with all governing laws, regulations, RevMed standard operating procedures (SOPs), and other guidelines.
• Independently represent Safety Science at cross-functional team meetings.
• Contribute to the development of SOPs and Safety Science processes.

Requirements

• A relevant postgraduate qualification (e.g., MD, PharmD, PhD/MSc in a Life sciences discipline, or other post-graduate health professional qualifications).
• 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 foster positive partnerships.
• Broad understanding of the scientific aspects of safety, pharmacovigilance (PV) (including GVP, GCP), and clinical/patient risk management and safety operations.
• Demonstrated ability to lead and influence, with and without authority, in a fast-paced environment.
• Strong presentation skills, effective at summarizing and presenting key considerations and decision points.
• Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high-energy environment.
• Detail-oriented with the ability to prioritize tasks and function independently as appropriate.
• Strong organizational skills and an ability to interpret, discuss, and report trial-level data effectively and identify trends.
• Excellent written and verbal communication skills.

Pay

The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is $186,000 - $233,000 USD. The range displayed is intended for individuals working onsite in Redwood City and will be adjusted for the local market where a candidate is based. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.