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Oversee clinical trial quality and compliance for a biotech firm developing cancer therapies, ensuring adherence to GCP standards and regulatory requirements.
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 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.
Principal Statistical Analyst at Revolution Medicines designs and validates SAS-based clinical datasets and reports for oncology trials, ensuring CDISC compliance and regulatory submission readiness.
Leads oncology clinical trials for a biotech firm, overseeing operations, budgets, and cross-functional teams to advance novel cancer therapies.
Senior Product Manager to lead chemistry-focused product strategy, workflows, and AI-enabled tools for oncology drug discovery at a late-stage clinical biotech company.
Oversee global GxP document control for a biotech firm, ensuring compliance with regulatory standards while managing document lifecycles and workflows in an electronic system.
Senior Machine Learning Scientist in drug discovery, building AI models to predict drug efficacy and toxicity using Python, PyTorch, and cheminformatics tools.
Oversee Japan’s regulatory strategy for oncology drugs, interfacing with PMDA and global teams to guide clinical development, submissions, and approvals for RAS-targeted therapies.
Evaluates and oversees drug safety data for cancer therapies, ensuring compliance with global regulations and protecting patient welfare through medical review of adverse events and regulatory submissions.
Senior ML scientist builds predictive models and analytics to accelerate drug discovery for RAS-addicted cancers, integrating biological, chemical, and structural datasets using deep learning and cheminformatics tools.
Senior architect designs and configures Veeva Vault CRM and related field platforms for a biotech company, integrating APIs and ensuring compliance in a regulated life-sciences environment.
Principal Infrastructure Security Engineer at Upstart designs and implements secure-by-default cloud and platform controls, automating security across AWS, Kubernetes, and CI/CD to reduce systemic risk for a leading AI lending marketplace.
Senior Salesforce Developer builds and expands Salesforce platforms for real estate tools, focusing on Sales, Service, and Marketing Cloud with Agentforce AI integrations.
Leads the design system and team for Avail, Realtor.com’s rental platform, defining components, patterns, and accessibility standards while managing designers and collaborating with engineering to scale the product.
Lead a new partner marketplace platform for Realtor.com, building a data ingestion ecosystem to feed AI models and enterprise revenue streams while managing legal, financial, and technical guardrails.
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