Clinical Research Coordinator: Study Operations & Compliance

The University of Texas Medical Branch; Galveston (TX); On-site; USD 55,000 - 75,000; Full time

Job summary

The University of Texas Medical Branch (UTMB Health) is seeking a Clinical Research Coordinator to collect human subject data for clinical studies and perform general administrative duties to support research activities.

The role involves coordinating site visits, maintaining source documents, assisting with IRB submissions, and ensuring protocol compliance under PI direction. Strong organizational skills and knowledge of GCP are preferred.

Qualifications

• Bachelor's degree or equivalent, and two years of directly related experience.

Responsibilities

• Applies knowledge in contributing to Good Clinical Practice (GCP) activities and/or other regulatory activities.
• Schedules, coordinates, and participates in the pre-site visit and site initiation visits; coordinates study initiation.
• Maintains and monitors source documentation and appropriate forms as per protocol for quality and accuracy, including participant records; assists with the quality assurance process.
• Incorporates directions from other health care disciplines into clinical research protocols when reviewing patient eligibility; assists in eliciting relevant data from sources outside of the hospital.
• Reconciles study drug accountability; maintains temperature and QC logs per protocol compliance.
• Develops and maintains productive working relationship with the study monitor; attends and participates in campus coordinator workshops.
• Identifies and recruits clinical research subjects for participation of studies, collects data, and monitors enrollment goals.
• Mentors new clinical research coordinators and assistant clinical research coordinators.

Education

Bachelor's degree or equivalent

Job description

The University of Texas Medical Branch (UTMB Health) is seeking a Clinical Research Coordinator to collect human subject data for clinical studies and perform general administrative duties to support research activities.

The role involves coordinating site visits, maintaining source documents, assisting with IRB submissions, and ensuring protocol compliance under PI direction. Strong organizational skills and knowledge of GCP are preferred.