Day-to-Day Responsibilities
Plans the trial timeline, milestones and resources with the study team
Coordinates with clinical sites, investigators and hospital staff to start and run the study
Tracks enrolment of volunteers and flags delays to the sponsor early
Monitors budgets, vendor contracts and study costs
Ensures the trial follows Good Clinical Practice and the rules set by regulators
Reviews data quality and reports on safety and progress to the sponsor
Leads and guides clinical research associates, coordinators and data staff


