ImmunityBio, Inc.

General

• Respond to and resolve escalated medical and safety information inquiries from consumers, healthcare professionals, and external customers
• Compose and update standard response documents and obtain Medical, Legal, and Regulatory approval
• Research and write custom medical information responses
• Support development of medical information SOPs
• Provide labeled and unlabeled efficacy, safety, and scientific information in accordance with regulatory requirements and industry standards
• Identify, document, and report adverse events, special situation events, and product complaints to Pharmacovigilance
• Review and confirm eligibility for clinical trial programs and connect patients or caregivers with appropriate trial contacts
• Create medical materials for patients, healthcare providers, and population health decision makers
• Participate as a medical reviewer in Promotional Review Committee and Medical Review Committee activities
• Support clinical operations across ImmunityBio’s oncology portfolio
• Document, triage, and fulfill medical information inquiries
• Troubleshoot medical information database vendor issues
• Generate medical information metrics and reports
• Adhere to privacy and data protection policies
• Perform other assigned activities

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