Manages research project databases
develops flow sheets and other study related documents
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
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
Prepares regulatory submissions.
With appropriate credentialing and training may perform phlebotomy or diagnostics.

High School Diploma or GED and five years of clinical research experience
two years of college in a scientific, health related, or business administration program and three years clinical research experience
licensed as a practical nurse (LPN) and two years clinical research experience
Bachelor's degree in a scientific, health related, or business administration related program and one year of clinical research experience
Master's degree, MD or PhD in a scientific, health related or business administration program.

Clinical Research Coordinator II

About this role