Regional Monitor (CRA)

Overview

REGIONAL 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

Location

Work will be performed remotely from home and at study sites in the Eastern United States