Clinical Research Study Assistant I (Time-Limited) - Program in Physical Therapy

Requirements

• Following training, assists with data collection and processing as directed by PI or research coordinator.
• Maintains and updates site demographics on computer database; logs forms received and file as appropriate; prepares reports from database to include weekly reports and other reports as requested.
• Receives and disseminates study-related regulatory documents and correspondence; assists in screening documents for completeness and compliance with protocol and appropriate regulations; assists in investigating incomplete, inaccurate or missing documents to ensure accuracy and completeness of data.
• Communicates and coordinates with other study personnel as required for study implementation and routine problem resolution.
• Attend routine meetings and other meetings related to clinical research; stays abreast of information and any changes to study protocol.

Benefits

• Paid Time Off
• 401k Matching
• Health Insurance