Jobs at Artiva Biotherapeutics

Support Quality Assurance operations with a focus on document control, records and training management, controlled labeling, and archival/digitization of quality records. Maintain inspection-ready documentation in the eQMS, assist onboarding and audits, monitor document review cycles, and provide guidance to document authors while ensuring compliance with FDA, ISO, ICH, EU GMP, and internal procedures.

Lead corporate development and long-range strategy for a clinical-stage NK cell therapy company. Drive pre-launch commercial planning, publication strategy, investor and board materials, fundraising support, and BD diligence and deal support. Collaborate cross-functionally with clinical, medical, finance, and executive teams to translate scientific data into commercial strategy and stakeholder-ready narratives.

Develop and run translational immunology assays (flow cytometry, cytokine profiling, cytotoxicity, ddPCR/qPCR), process clinical biospecimens, analyze and report data, and lead assay transfers and troubleshooting with CROs to support clinical trials.

Manage end-to-end contract lifecycle for commercial and clinical agreements, including drafting, negotiation, execution, and obligation tracking. Partner with business, Finance, Procurement, and CROs on clinical trial agreements and playbooks. Lead CLM selection/implementation, support data privacy and legal operations, identify and escalate contractual and compliance risks.

The Manager, Biomarker Operations oversees clinical biomarker project operations, coordinating sample management, vendor deliverables, and communication between internal and external stakeholders to ensure successful trial execution.

The Senior Director, Safety and Pharmacovigilance leads Safety and PV activities, ensuring compliance with regulations, overseeing adverse event reporting, and managing vendor relationships.

The Senior Associate, QA Compliance is responsible for overseeing quality assurance compliance, managing deviations, CAPAs, change controls, and supporting audits in an FDA regulated environment.

The Associate Director/Director will lead translational science for clinical development in autoimmune diseases, overseeing pharmacology, biomarker strategies, and CRO management.