Orca Bio is revolutionizing allogeneic cell therapy with next-gen therapies for better outcomes and fewer risks, transforming lives through precision and innovation.
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Orca Bio is seeking a Manager, Quality, Commercial Site Onboarding to lead East Coast commercial partner onboarding, ensuring treatment centers are prepared for compliant, efficient, and successful ongoing operations.
Orca Bio is seeking a National Senior Director of Field Medical Affairs to lead and expand its field-based MSL organization supporting next-generation cell therapies for blood cancer, aligning medical strategy with compliant execution across U.S. territories.
Orca Bio is seeking a Coordinator, Commercial Marketing & MLR to manage commercial marketing operations and coordinate compliant promotional and medical review workflows for its cell therapy programs.
Orca Bio is seeking a Southeast US Account Director to lead payer and health-system market access strategy, secure favorable coverage and reimbursement for its cell therapies, and support treatment-center onboarding and patient access.
Orca Bio is seeking a Director of Trade, Distribution and Patient Assistance to build and operate the U.S. distribution channel for its cell therapy portfolio, ensuring products move reliably from the company to authorized treatment centers and patients.
Orca Bio is seeking a Senior Director, Field Market Access to lead U.S. payer account teams and advance access, reimbursement, pricing, and commercialization strategies for TREGZI and future indications.
Orca Bio is hiring a Clinical Research Associate to monitor oncology and cell therapy clinical trials remotely and at investigative sites, ensuring study execution, documentation, and reporting comply with protocols, SOPs, ICH-GCP, and applicable regulations.
Orca Bio is seeking a Director, Case Management to lead national case management operations for TREGZI, coordinating patient care across treatment centers while scaling post-launch service infrastructure.
Orca Bio is seeking a pharmacovigilance professional to review and manage adverse event data for investigational cell therapy products, supporting accurate regulatory reporting and patient safety.
