Clinical Research

• Manages research project databases, develops flow sheets and other study related documents, and completes source documents/case report forms
• Provides guidance to less experienced staff
• Interfaces with research participants, determines eligibility and consents study participants according to protocol
• Approves orders for supplies and equipment maintenance
• Assists in developing recruitment strategies and conducting screenings for study participants including interviews and questionnaires
• Supervises collection of study specimens and processing
• Establishes case packages for study procedures, monitors scheduling of procedures and charges, coordinates other services as needed
• Ensures compliance with research protocols, reviews case report forms and audits for accuracy with source documents, attends monitoring meetings with sponsors
• Prepares regulatory submissions
• With appropriate credentialing and training may perform phlebotomy or diagnostics.
• Performs related approved responsibilities as required.

Clinical Research Coordinator II – Emergency Medicine

Clinical Research Coordinator III – Psychiatry

Clinical Research Data Coordinator I

Biostatistician – Temporary Full-Time

Clinical Research Coordinator III – Palliative Medicine

Clinical Research Coordinator III – Palliative Medicine