Description
We are seeking a Regional Medical Advisor to serve as a key medical expert on assigned projects.
As a Regional Medical Advisor, you will primarily serve as a Regional Medical Advisor on assigned projects and provide scientific guidance to Project Leaders on medical and scientific aspects.
Key responsibilities include:
- Providing medical support to investigative sites and project staff for protocol-related issues, including protocol clarifications, inclusion/exclusion determinations, and patient safety and eligibility issues
- Performing medical review of protocols, Investigative Drug Brochures (IDBs), and Case Report Forms (CRFs)
- Providing therapeutic area/indication training for project clinical teams
- Attending and presenting at Investigator Meetings
- Reviewing and clarifying trial-related Adverse Events (AEs)
- Collaborating with the Pharmacovigilance department on medical case reviews of Serious Adverse Events (SAEs) and Analysis of Similar Events (AOSE)
- Reviewing adverse event coding and Clinical Study Reports (CSRs) and patient narratives
- 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, and involves repetitive motion of fingers and accurate perception of speech.