OverviewREGIONAL MONITOR (18-months, Possibility of Extension)
Duties & Responsibilities:
Site communications and scheduling and conducting monitoring visits at clinical study sites.
Team meetings and communications
Study document review
Preparing and editing visit reports within the allotted timeframe
Other duties, as required.
Qualifications & Requirements:
5+ years of experience as a Regional Monitor CRA, including a minimum of two years of ophthalmology drug trials
Familiarity with ICH, GCP and FDA guidelines and requirements
Good written, verbal and interpersonal communication skills & solid computer skills
LocationWork will be performed remotely from home and at study sites in the Eastern United States
