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Artiva Biotherapeutics
Director / Sr. Director, Clinical Development
Remote · United States · Full time · Senior level
$250k–$350k / year
About the role
Provide medical oversight and safety monitoring across clinical trials ensuring participant safety and regulatory compliance. Collaborate across functions in a fast-moving biotech environment.
What you’ll do
• Provide ongoing medical monitoring and safety oversight for clinical trials. • Serve as primary medical contact for investigators and sites. • Review and assess adverse events and support safety signal detection. • Provide clinical input into protocols and study documents. • Support readiness for audits, inspections, and regulatory review.
What you’ll bring
• MD required. • Hands-on medical monitoring in Phase 2-3 rheumatology or immunology trials. • Background in immunology, autoimmune disease, rheumatology or cell therapy. • 5+ years clinical development or medical monitoring experience. • Familiarity with regulatory submissions and health authority interactions.
Life at Artiva Biotherapeutics
Entrepreneurial, collaborative, and innovative environment with comprehensive benefits including medical, dental, vision, 401(k), PTO, and recognition program.
About Artiva Biotherapeutics
Clinical-stage biotechnology company developing natural killer cell-based therapies for autoimmune diseases, focusing on safe and accessible treatments.