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Owns and strategizes Hippo’s insurance product platform, including rating/pricing engines, coverage logic, and business rules, driving long-term tech infrastructure improvements while ensuring compliance, profitability, and competitive positioning in insurance tech.
Title : Director, Program Business Location : Morristown, NJ / Dallas, TX / Austin, TX / San Jose, CA Reports To : Chief Program & Underwriting Officer, Spinnaker About Hippo: Hippo was built on a promise: make…
Turning Space into a Transportation Layer for Earth Who We Are: Inversion builds advanced reentry systems to deliver next-generation capabilities from space. Our mission is to make Earth radically more accessible by…
Provide high-level executive support to leadership at a space-transportation startup, handling complex calendars, travel, board coordination, and sensitive operations in a fast-paced aerospace environment.
Job Description Primary Function of Position We are seeking a strategic privacy compliance and operations individual contributor to help shape and scale Intuitive’s global privacy program. This role partners across all…
Electrical Test Engineer at Saronic (Austin, TX) develops and executes electrical test plans and builds automated test equipment to validate PCBAs, harnesses, power systems, and assemblies for autonomous maritime vehicles. Day to day involves test scripting (Python/LabVIEW/MATLAB), lab instrumentation, troubleshooting, and cross-functional collaboration.
Coordinates supplier quality issues for a food manufacturer, sampling materials, verifying labels, and tracking defects to ensure compliance with standards.
Company Overview ID.me is the next-generation digital identity wallet that simplifies how individuals securely prove their identity online. Consumers can verify their identity with ID.me once and seamlessly login…
Oversee Japan-based accounting operations for a biotech firm preparing for commercial launch, including GAAP compliance, ERP systems, and OTC processes.
Oversee internal projects and operational improvements for a biotech firm developing targeted cancer therapies, partnering with clinical teams to streamline processes and tools.
Oversee clinical trial quality and compliance for a biotech firm developing cancer therapies, ensuring adherence to GCP standards and regulatory requirements.
Oversee global regulatory submissions and project plans for oncology drugs, coordinating cross-functional teams to meet compliance and approval timelines.
Lead statistical design and analysis for oncology clinical trials, real-world evidence, and health economics studies using SAS/R, while partnering with cross-functional teams to generate data-driven insights for RAS-targeted cancer therapies.
Oversee oncology clinical trials for a biotech firm, ensuring compliance with regulations and managing cross-functional teams to deliver therapies for RAS-addicted cancers.
Oversee Good Laboratory Practice (GLP) compliance for a clinical oncology company, auditing internal and external vendors to ensure regulatory adherence for RAS-targeted cancer therapies.
Leads statistical analysis and data science for oncology drug development, designing models, mentoring teams, and supporting regulatory submissions using SAS/R.
Leads global regulatory filings for late-stage oncology drugs, coordinating cross-functional teams to prepare and submit NDA/MAA applications under expedited pathways.
Leads US regulatory filings (NDA/MAA) for late-stage oncology drugs, coordinating cross-functional teams and advising on expedited pathways to secure approvals for RAS-targeted therapies.
Leads global GCP QA strategy for late-stage oncology clinical trials, ensuring regulatory compliance, audit readiness, and patient safety while overseeing vendor quality and inspection outcomes.
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)…
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