Monitor multiple Phase II/III clinical trial sites, across therapeutic areas. Assist other CRA with co-monitoring activities both remote and on-site as needed. Target 5-10 site assignments (depending on complexity/enrollment/stage of study), average 2-3 protocols and 1-2 therapeutic areas at any given time. The number would be adjusted based on the workload assignment.
Requirements: -Must have a Bachelor's Degree (or equivalent) -Minimum 1 years of monitoring and site management experience. -English is workable, along with proficiency in the use of Microsoft Office suite.
