Supports and assists in all aspects of clinical data management
Primary Data Coordinator for therapeutic and non-therapeutic clinical trials across all disease teams
Reviews information from medical records to extract data for assigned research protocols
Accurately captures and enters data into clinical trial databases
Collects and maintains complete records and metrics on each research study participant
Consolidates clinical data and reports for investigators as needed
Attends study team meetings and provides updates to study team members regarding protocol data management activities
Attends protocol related training meetings and completes all required study training
Prepares for and assists with internal quality control audits to verify the accuracy, completeness, and confidentiality of research data
Reports and addresses findings as appropriate
Provides support during internal and external monitoring and auditing
Assists in the establishment and maintenance of procedures and systems for research coordination and data management
Assures ongoing compliance with all departmental, institutional, and federal requirements and regulations
Maintains controls to assure accuracy, completeness, and confidentiality of research data
Maintains confidentiality standards for all potential and enrolled study participants; complies with federal Health Insurance Portability and Accountability Act (HIPAA) regulations.

High School Diploma or GED and three years of administrative support experience
Or two years of college in a scientific, health related, or business administration program and one year of admin support or customer service experience
Or licensed as a practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience
Or bachelor's degree, Master's degree, MD or PhD in a scientific, health related or business administration program.

Clinical Research Data Coordinator I

About this role