Description
We are seeking a Regional Medical Advisor to serve as a primary medical expert on assigned projects.
As a Regional Medical Advisor, you will provide 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.
Key responsibilities include:
- Providing medical review of protocols, Investigative Drug Brochures (IDBs), and Case Report Forms (CRFs)
- Offering therapeutic area/indication training for project clinical teams
- Attending and presenting at Investigator Meetings
- Reviewing and clarifying trial-related Adverse Events (AEs)
- Performing medical case reviews of Serious Adverse Events (SAEs) in collaboration with the Pharmacovigilance department
- Providing medical support for the Analysis of Similar Events (AOSE)
- Reviewing adverse event coding and Clinical Study Reports (CSRs)
- Participating in Kick-Off meetings, weekly team meetings, and client meetings as needed
- Being available 24/7 to respond to urgent protocol-related issues at investigative sites
- Traveling regularly as required
This role requires extensive use of keyboard, telephone, and face-to-face communication, with accurate perception of speech.
IQVIA creates intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.