Clinical Research Coordinator III

3 days ago


Albuquerque, New Mexico, United States DM Clinical Research Full time
Job Overview

We are seeking a highly skilled Clinical Research Coordinator III to join our team at DM Clinical Research. As a key member of our research team, you will be responsible for ensuring the quality and integrity of clinical research studies at assigned investigative sites.

Key Responsibilities
  • Ensure compliance with sponsor protocols, FDA regulations, and ICH/GCP guidelines
  • Conduct and oversee study subject visits, and all other relevant protocol-required procedures
  • Adhere to ALCOA-C standards with all clinical trial documentation
  • Complete and oversee data entry and query resolution in a timely manner
  • Liaise with laboratory team, data team, administrative staff, clinical investigators, research participants, and sponsor/CRO representatives
  • Maintain a working knowledge of current FDA regulations, ICH-GCP guidelines, and assigned study protocol(s)
  • Supervise visit preparedness for all relevant sponsor and CRO visits
  • Oversee reporting of adverse and serious adverse events and other relevant safety information
  • Strive to meet sponsor subject enrollment goals
  • Attend required company meetings and submit administrative paperwork on time
Requirements
  • High school diploma or equivalent required; bachelor's degree preferred
  • Minimum 5 years experience in clinical research; supervisory experience preferred
  • Wide therapeutic range of clinical trials experience preferred; regulatory research experience a plus
  • ACRP or equivalent certification preferred

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