Onsite Clinical Research Data Coordinator I

Posted yesterday

Apply now

About the role

  • Clinical Research Data Coordinator supporting clinical data management at Winship Cancer Institute. Assisting in clinical trials, maintaining records, and ensuring regulatory compliance.

Responsibilities

  • 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.

Requirements

  • 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.

Benefits

  • Health insurance
  • 401(k) matching
  • Paid time off
  • Flexible work arrangements

Job title

Clinical Research Data Coordinator I

Job type

Experience level

Mid levelSenior

Salary

Not specified

Degree requirement

High School Diploma

Location requirements

Report this job

See something inaccurate? Let us know and we'll update the listing.

Report job