**Essential Functions**
• The role includes predominantly Medical Monitoring responsibilities with Medical Strategic input involvement as requested.
• Medical Monitoring:

•Primarily serves as Global and /or Regional Medical Advisor on assigned projects.
•Serves as Scientific Advisor and provides guidance to Project Leaders on the medical and scientific aspects of assigned projects.
•Provides medical support to investigative sites and project staff for protocol-related issues including
protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility.
•Performs medical review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs).
•Provides therapeutic area/indication training for the project clinical team.
•Attends and presents at Investigator Meetings.
•Performs review and clarification of trial-related Adverse Events (AEs).
•May perform medical case review of Serious Adverse...