Current opportunities to be a part of a dynamic team
Plans, manages and coordinates the execution of clinical study/studies according to regulatory requirements and Vanguard Standard Operating Procedures for all site(s), nationwide. Ensures coordination between cross functional study team(s) to meet study objectives, on time and within budget. Provides study level updates, including timelines & budget, to management.
SITE CLINICAL RESEARCH MANAGER
Provides day-to-day management of research administration at a clinical site(s), nationwide, including monitoring the quality and accuracy of clinical trial data. Follows the established monitoring Standard Operating Procedures (SOP) and protocol specific monitoring plan.
Interested in knowing about future opportunities at VRG?
Sr. Administrative Director