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Clinical Research Coordinator I - DLD

Columbia University
Columbia University Medical Center
$63.7K-$75K a year
Full-time

Position Summary

We are seeking a Clinical Research Coordinator to join the Division of Digestive & Liver Disease within the Department of Medicine at CUIMC.

This role will be instrumental in coordinating the research activities of multiple ongoing projects, including NIH / NCI grant-funded studies and industry-sponsored clinical trials.

Our research focuses on upper gastrointestinal diseases, the microbiome's impact on GI disease development and progression, and the implementation of innovative screening methods for GI conditions.

Responsibilities

  • Oversee and maintain active IRB approval for assigned research protocols, submitting modifications and renewals as required.
  • Foster effective communication with the study team, research sites, and sponsors to ensure timely updates on protocol changes and study status.
  • Screen medical records to identify eligible participants based on specific inclusion and exclusion criteria. Contact potential participants to enroll them in the study.
  • Conduct study visits, administer questionnaires, collect and handle biological specimens, and maintain accurate and up-to-date research records and databases.
  • Serve as the primary point of contact for research participants, addressing inquiries, providing updates, and ensuring their satisfaction.
  • Work closely with departmental research personnel and other CUIMC departments, including Sponsored Projects Administration and the Clinical Trials Office.
  • Report directly to the Clinical Research Manager of the DLD research team and Principal Investigators of relevant studies.
  • Perform additional related duties as needed.

Minimum Qualifications

  • Requires a bachelor's degree or equivalent in education, training and experience, plus three years of related experience.
  • Minimum of two years of experience in a clinical research setting.

Preferred Qualifications

  • Bilingual (Spanish).
  • Experience in clinical settings, IRB submissions, GCP and HSP principles, and HIPAA regulations.
  • 11 hours ago
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