Job Description
Start your career in clinical research, streamlining communication, maintaining systems and managing documents.
The scope of responsibilities will include:
Main site contact for all non-trial-participant related and non-protocol
related issues, including vendors, trial supplies and access managementManages records flow with sites and off-site facilitiesPrepares regulatory and ethics committee submission/ notification
documents and recordsCoordinates payments to sites and off-site facilitiesPrepares for and follows up on site audits and inspectionsReviews and coordinates site-specific query resolution with Monitors and
sitesReviews site-specific EDC completion progress and provides the Monitor
with regular updatesServes as the main contact point for other company departments in
administrative site-related issuesOrganizes, ...