Senior Manager, Global Patient Safety Operations

Role overview The Senior Manager, Global Patient Safety Operations at Revolution Medicines plays a central role in protecting patient health and ensuring compliance with regulatory requirements. Based in Redwood City, California, this position leads efforts to monitor and improve patient safety practices across international operations. The Senior Manager gu…

Revolution Medicines, Inc. is hiring a Senior Manager of Global Patient Safety Operations to join the team in Redwood City, California. This leadership role centers on guiding patient safety operations and maintaining regulatory compliance across the organization’s global activities. What you will do Direct patient safety operations on a global scale, ensuring all processes meet regulatory requirements. Champion initiatives that strengthen a culture of safety and vigilance throughout the company. Collaborate with cross-functional teams to support and enhance patient outcomes. Location This role is based in Redwood City, California, United States.

Revolution Medicines, based in Redwood City, California, develops targeted therapies for patients with RAS-addicted cancers. The company’s pipeline includes several RAS(ON) inhibitors, each designed to address specific oncogenic RAS protein variants. Clinical candidates such as daraxonrasib (RMC-6236), elironrasib (RMC-6291), zoldonrasib (RMC-9805), and RMC-5127 are in development, all focused on improving outcomes for patients with RAS pathway mutations. Role overview The Senior Director of Global Patient Safety Science leads safety science and pharmacovigilance across all products in the Revolution Medicines portfolio. This position shapes safety oversight and sets strategic direction for both early and late-stage development. The role sits within the Global Patient Safety team and may include direct reports, depending on program assignments. The Senior Director guides multiple or complex development programs and works closely with cross-functional teams to deliver thorough safety assessments and risk management plans. What you will do Oversee safety surveillance and risk management activities, including medical review of Individual Case Safety Reports (ICSRs), routine safety data evaluations, and scientific literature reviews. Contribute to safety signal assessments and address inquiries from regulatory authorities. Provide medical safety expertise for the design and execution of pharmacoepidemiology and observational studies. Plan and interpret safety data, preparing and presenting comprehensive summaries to internal and external stakeholders. Develop in-depth knowledge of assigned products’ safety profiles, considering disease context, competitor data, and mechanisms of action. Remain accountable for benefit-risk safety profiles throughout the product lifecycle.

Role overview Corcept Therapeutics is hiring a Manager of Patient Safety & Pharmacovigilance Compliance based in Redwood City, California. This position focuses on strengthening patient safety processes and ensuring the company meets regulatory standards in pharmacovigilance. What you will do Lead projects and initiatives that raise patient safety standards throughout the organization. Monitor and enforce compliance with all applicable pharmacovigilance regulations and requirements. Create and present training programs to keep staff up to date on best practices and compliance expectations. Promote a culture centered on patient well-being by supporting education and process improvements.

Revolution Medicines, Inc. is seeking a highly skilled and passionate individual for the role of Executive Director, Global Patient Safety, Quality and Compliance - Pharmacovigilance. This pivotal position will lead our global efforts in ensuring the safety and compliance of our pharmaceutical products, emphasizing our commitment to patient welfare and regulatory standards.The ideal candidate will have extensive experience in pharmacovigilance, with a deep understanding of risk management and quality assurance within the pharmaceutical industry. This role requires a visionary leader who can navigate the complexities of global regulatory environments and inspire a team dedicated to excellence in patient safety.

Join Revolution Medicines as a Systems Analyst II in the Global Patient Safety, Systems & Analytics team. In this role, you will play a crucial part in enhancing our patient safety systems and analytics processes. You will work collaboratively with cross-functional teams to identify requirements, analyze data, and implement solutions that support our mission of improving patient outcomes across the globe.

Revolution Medicines develops targeted therapies for patients with RAS-addicted cancers. The company’s pipeline includes several RAS(ON) inhibitors currently in clinical development, such as Daraxonrasib (RMC-6236), Elironrasib (RMC-6291), Zoldonrasib (RMC-9805), and RMC-5127. The team is dedicated to advancing treatments for cancers driven by mutations in the RAS signaling pathway. Role overview The Senior Safety Scientist will join the Global Patient Safety Science group, supporting pharmacovigilance and safety science activities across both early and late-stage clinical programs. This position covers the full portfolio of Revolution Medicines’ investigational therapies. Key responsibilities Oversee safety for clinical studies, including reviewing and authoring protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), and Development Safety Update Reports (DSURs). Conduct medical review of individual case safety reports (ICSRs) and monitor safety surveillance for assigned products. Proactively perform medical safety surveillance during clinical trials to identify and address safety issues. Prepare and present safety data summaries to internal and external stakeholders. Engage in risk management activities, including routine safety data analysis, medical review of ICSRs, and literature review. Share knowledge on drug class safety issues and competitor landscape. Identify potential clinical safety concerns and recommend risk mitigation strategies. Contribute to preparation and maintenance of clinical trial protocols, IBs (including reference safety information), ICFs, DSURs, Risk Management Plans (RMPs), Core Content Development Summaries (CCDS), and product labeling. Review clinical protocols, IBs, ICFs, and related documents to ensure alignment with safety strategies. Location This role is based in Redwood City, California, United States.

About Zūm:Zūm is at the forefront of transforming mass mobility through its innovative Connected Mobility Experience (Zūm CMX™) system, which seamlessly connects and coordinates people, vehicles, and operations in real time. Operating within the expansive $50 billion student mobility market—the largest segment of the mass mobility industry—Zūm CMX is redefining what has historically been a source of anxiety and disruption into a dependable, transparent, and efficient mobility solution for students and their families. Currently, over 4,500 schools trust Zūm CMX for their transportation needs. Zūm's groundbreaking methods and operational excellence have earned it recognition on numerous prestigious lists, including Fast Company’s World’s Most Innovative Companies, CNBC’s Disruptor 50, and the Financial Times’ Fastest Growing Companies. With support from leading investors such as Sequoia Capital, GIC, TPG, and Softbank, Zūm is poised for continued growth and impact.

Join Poshmark Inc. as a Senior Manager of Operations Analytics, where you will play a pivotal role in driving data-driven decisions that influence our operational strategy. You will lead analytical projects, providing insights to optimize our processes and enhance overall performance.

Join Revolution Medicines, a pioneering biopharmaceutical company dedicated to transforming the lives of patients through innovative therapies. We are seeking a highly accomplished and motivated Senior Director of Global Commercial Development to lead our commercial strategy and maximize the value of our product portfolio.In this critical role, you will spearhead global commercial initiatives, providing strategic direction and oversight for market access, product launch, and commercial operations. You will collaborate with cross-functional teams to identify opportunities for growth and ensure alignment with corporate objectives.

Revolution Medicines, Inc. is seeking a highly skilled and experienced Senior Manager of Regulatory Operations with a focus on Records & Information Management. In this pivotal role, you will lead efforts to ensure compliance with regulatory requirements and enhance the efficiency of our records management processes. You will collaborate closely with cross-functional teams to develop and implement strategies that align with our corporate objectives and support our mission of advancing innovative therapies for patients.

As a Senior Program Manager in Vendor Operations at Chan Zuckerberg Initiative, you will play a pivotal role in optimizing our vendor management processes. You will lead strategic initiatives to enhance operational efficiency and ensure the alignment of vendor services with organizational goals. The ideal candidate will leverage their expertise in program management to foster strong relationships with vendors while driving continuous improvement in service delivery.

At Carbon, we transcend the boundaries of traditional 3D printing to empower creators globally to produce what the world demands today. Our ethos centers on the collaboration of diverse disciplines to tackle complex challenges. With ambitious goals, we aim to develop technology that will reshape industries worldwide. Join a dynamic team that values a vibrant culture, where collective success is celebrated alongside individual achievements. Help us revolutionize the world, and we will assist you in transforming yours.As an experienced professional, you will take charge of the comprehensive category strategy for our intricate Light Engine and electronics portfolios. In this managerial capacity, you will operate with a significant degree of autonomy, converting complex business requirements into a cohesive global sourcing strategy. Your contributions will have a direct effect on our operational processes and product scalability, ensuring that we not only meet current demand but also anticipate future needs.This position is Hybrid, requiring a minimum of three days a week in our Bay Area, CA office.Strategic Impact & ResponsibilitiesCategory Architecture: Oversee the complete lifecycle of Light Engines, PCBA, Cables, and accessories categories. You will establish long-term business cases, supplier selection criteria, and executive alignment, guiding the team from reactive strategies to proactive, multi-year plans.Complex Negotiations & Commercial Excellence: Spearhead high-stakes negotiations for MSAs, NRE, and open-book pricing. You will create advanced cost models and risk-buy frameworks that significantly enhance the company’s financial performance.Supply Chain Resilience & Compliance: Develop and expand a global supply network. This includes mapping sub-tier suppliers and raw materials to ensure compliance and resilience across the supply chain.Innovation through AI & Automation: Proactively identify and implement AI-driven tools or automated workflows to reduce repetitive manual tracking. You will advocate for the use of technology to enable your (and your team’s) focus on high-value strategic initiatives.Cross-Functional Influence: Convert engineering requirements into actionable sourcing strategies. Collaborate with Engineering, Finance, and Program Management at all levels to ensure our supply readiness aligns with significant growth milestones.Mentorship & Leadership: As a leader within the team, you will mentor colleagues, share your professional network, and exemplify our “Ways of Working,” elevating the entire Operations organization.

About Box Box (NYSE: BOX) stands at the forefront of Intelligent Content Management. Our innovative platform empowers organizations to enhance collaboration, oversee the entire content lifecycle, safeguard essential information, and revolutionize business processes through enterprise AI. Founded in 2005, we simplify operations for top global organizations such as JLL, Morgan Stanley, and Nationwide, with our headquarters located in Redwood City, CA, and offices across the United States, Europe, and Asia. Joining Box offers a unique opportunity to propel our platform's evolution. Content is the lifeblood of how we operate, encompassing billions of files and data exchanged daily across teams, departments, and vital business processes—ranging from contracts and invoices to employee records and marketing assets. Our mission is to infuse intelligence into content management, enabling our customers to completely revamp their workflows. The integration of AI with enterprise content presents an unprecedented opportunity to enhance collaboration, and at Box, you'll be at the forefront of this transformative journey. Why Box Needs You As Box undergoes rapid expansion, organizations worldwide are reimagining content management. Positioned as a leader in Intelligent Content Management, Box is dedicated to driving transformative change. Our Professional Services division is set for significant growth, and we are eager to find an exceptional leader in operations strategy to expedite this trajectory. In this pivotal role, you will work at the intersection of strategy and execution, defining how Box delivers value to its customers through our services organization. You will collaborate closely with Consulting leadership, Finance, Revenue Operations, and other go-to-market teams to ensure our organization runs efficiently and profitably while aligning with company goals. Leading a high-performing team focused on forecasting, planning, reporting, and process optimization, you will be the operational backbone that allows our services business to scale effectively and achieve remarkable customer outcomes. Your contributions will directly shape how we plan, deliver, and grow our Professional Services business, ensuring operational excellence as we continue to expand. Your Responsibilities Collaborate with Box Consulting leadership...

For over 25 years, Corcept Therapeutics has been dedicated to advancing the understanding of cortisol, a crucial hormone that, when dysregulated, contributes to various diseases.Our innovative commercial portfolio comprises treatments for hypercortisolism and oncology. With over 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists discovered, we are engaged in advanced clinical trials for conditions such as hypercortisolism, solid tumors, ALS, and liver disease. At Corcept, we are harnessing the potential of cortisol modulation to combat some of the most challenging health issues faced by patients today.Based in Redwood City, California, we invite you to explore more at www.corcept.com.The Senior Manager of Privacy Operations will lead the implementation, operationalization, and continuous enhancement of Corcept’s global privacy program. This role involves translating legal and regulatory privacy requirements into effective, scalable, and auditable operational processes throughout the organization.This position requires close collaboration with IT, HR, Clinical, Commercial, Drug Safety, and Quality functions to ensure that privacy requirements are integrated into daily business activities, systems, and vendor relationships. The ideal candidate will have robust experience in privacy program management and be adept at working hands-on in a regulated pharmaceutical environment. This role also provides the opportunity to engage with broader compliance topics.This is a hybrid position, typically requiring on-site presence three days a week.This role reports to the Senior Director of Legal & Privacy.

Revolution Medicines, Inc. seeks a Safety Scientist based in Redwood City, California. This role centers on supporting the safety and effectiveness of therapies under development. The Safety Scientist works with colleagues from various disciplines to review safety data, conduct evaluations, and assist with regulatory filings. What you will do Work with internal teams to assess and monitor safety profiles of therapies in development. Analyze safety data from both clinical and preclinical studies. Help prepare documents needed for regulatory submissions. Role impact This position plays a part in shaping new therapies and influencing the future of medicine by ensuring careful safety evaluation and strong collaboration across teams.

About the RoleCharacter.AI is seeking a passionate and innovative Software Engineer to join our Safety Engineering team! In this pivotal role, you will collaborate closely with Product, Design, and Trust and Safety operations teams to develop tools and product features that promote a safe, transparent, and engaging user experience. You'll be instrumental in crafting groundbreaking solutions to the unique challenges associated with human-to-AI interaction, applying your technical skills to help shape industry best practices in this evolving field.Key ResponsibilitiesDesign and implement the user interface for our Trust and Safety systems, balancing risk reduction, user experience enhancement, and platform reliability across various features to deliver an exceptional user experience.Gain a deep understanding of our users and their behaviors to create innovative technical solutions that encourage positive interactions on our platform.Partner with other product teams to co-create modular and scalable safety design systems that ensure all product features can be launched safely while maintaining a high launch velocity.Work collaboratively with the Trust & Safety team to understand moderation workflows and develop tools that enhance their decision-making capabilities. Evaluate and integrate third-party solutions when necessary.Collaborate with engineers and Trust & Safety stakeholders to design interfaces and interaction models that incorporate AI-assisted moderation, facilitating effective human-AI collaboration.Utilize user data and insights to enhance our core LLM and other models. Develop frontend systems that visualize the feedback loops between moderation actions and AI training, ensuring that critical data insights are surfaced to support safe and positive user experiences across the platform.

About DexterityAt Dexterity, we are passionate about the transformational potential of robotics. Our innovative technology empowers individuals to engage in creative and complex problem-solving tasks, allowing robots to take on repetitive and physically demanding work. We are initially focusing on warehouse automation, where the demand for smarter and more resilient supply chains significantly impacts millions of lives and businesses globally.Dexterity’s advanced robotics systems are designed to pick, move, pack, and collaborate with a level of skill, awareness, and learning akin to humans. Our solutions are software-focused and hardware-independent, having already processed over 15 million items in production. Our customer-centric approach drives every decision we make, ensuring that we empower our clients to achieve more with our robotic solutions than they ever imagined possible.As one of the fastest-growing firms in the robotics sector, Dexterity is proudly supported by prestigious investors including Kleiner Perkins, Lightspeed Venture Partners, and Obvious Ventures. Our diverse and multidisciplinary team thrives on a culture of passion, trust, and commitment. Join us at Dexterity and contribute to turning intelligent robots into a reality!About the RoleIn the capacity of a Senior Functional Safety Engineer, you will spearhead the design and verification of functional safety in our robotic systems while ensuring compliance with regulations in North America, Europe, and Japan. We are seeking a candidate with a comprehensive understanding of relevant industry standards, who can harmonize innovative engineering practices with established design and safety principles in this burgeoning field. Your contributions will be pivotal to Dexterity’s growth and global reach, as you design and implement safe and compliant solutions.

Box, Inc. is hiring a Legal Operations Manager in Redwood City, CA. This position focuses on improving legal processes and supporting compliance efforts across the organization. Role overview The Legal Operations Manager works closely with the legal team to refine workflows and introduce practices that improve efficiency. The role centers on identifying areas for process improvement and helping the team meet regulatory requirements. Key responsibilities Optimize legal operations and procedures Support compliance with relevant regulations Collaborate with legal professionals to implement process improvements What to expect This role involves both hands-on process work and strategic planning. The Legal Operations Manager will help shape how the legal department functions and contributes to the company's goals.

About the RoleWe are seeking a highly skilled and experienced Senior Manager of Clinical Business Systems to lead our dynamic team at Revolution Medicines. In this pivotal role, you will be responsible for overseeing the development and implementation of clinical business systems that ensure the efficiency and effectiveness of our clinical operations.Key ResponsibilitiesDesign, develop, and manage clinical business systems to support clinical trial operations.Collaborate with cross-functional teams to integrate clinical system solutions that enhance data quality and regulatory compliance.Provide leadership and mentorship to team members, fostering a culture of innovation and continuous improvement.Monitor industry trends and technologies to identify opportunities for system enhancements.