Clinical Research

• Independently manages significant aspects of clinical trials
• Trains and provides guidance to staff
• Oversees data management for research projects
• Interfaces with research participants and resolves study protocol issues
• Authorizes purchases for supplies and equipment maintenance
• Determines strategies for promoting/recruiting research participants
• Periodically audits operations for compliance
• Monitors IRB submissions and responds to requests
• Interfaces with study sponsors and resolves study queries
• Provides leadership in recommending and implementing improvements
• Assists in developing grant proposals and protocols
• May perform phlebotomy, specimens collection, or diagnostics

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