Senior Clinical Research Associate - (Cranford, NJ)

POSITION OBJECTIVE: Work within a clinical team setting to ensure compliance with protocol and overall clinical objectives. Essential Job Functions/Responsibilities Participates in the preparation and/or review of draft protocol and informed consent documents Possesses detailed knowledge of the study protocol and its associated activities and timelines Participates in conference calls, prepares agenda and summaries Coordinates with project team and other study personnel to determine data collection requirements based on protocol and to test electronic case report forms May review and contribute to, and processes project documents and required reports, such as study protocol documents and consent forms, SAE and protocol deviation reports, accrual and other study status and/or study site reports Contributes to project-specific site initiation activities, tracks readiness status of sites for study initiation, (e.g., submission of essential documents