Manages research project databases
Develops flow sheets and other study related documents
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
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 of 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

Health and safety information
Work with human blood, body fluids, tissues, or other potentially infectious materials

Clinical Research Coordinator II

About this role