This physician will serve as sub-investigator or primary investigator for Clinical Pharmacology and Phase 1 clinical studies. They will monitor and summarize clinical adverse events; maintain all aspects of medical safety for product lines and will provide medical review of safety protocols, and clinical brochures. This role is for a physician US Board Certification in Internal Medicine, Emergency Medicine or Family Medicine. They must hold an active US License that is transferable to State of Illinois within 3 months. This role role is for someone with minimum of 3 year of clinical experience within a pharmaceutical company, or CRO setting, related to clinical pharmacology or early phase clinical development. Familiarity with FDA organization, and experience with FDA inquiries involving drug safety and efficacy including the ability to review safety and labeling protocols is required.
