Coord Clinical Research (SIVS Operations Research - Galveston)

$34,960 - $52,440/Yr

The University of Texas System - Galveston, TX

Full-time - Mid Level

Galveston, TX

Educational Services

About the position

The Clinical Research Coordinator at UTMB Health is responsible for obtaining human subject data for clinical research activities, ensuring compliance with Good Clinical Practice (GCP) and regulatory standards. This role involves coordinating study initiation, maintaining documentation, recruiting participants, and supporting the Principal Investigator (PI) in various research-related tasks.

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.
• Assists with grant/protocol preparation and submission to IRB, OCR or OSP under direction of research coordinator under the direction of the PI and with answering IRB stipulations to obtain final approval; documents IRB approval and contract approval.
• Under direction of PI may draft various communications with Sponsor and/or regulatory documents to be sent to the Sponsor.
• May assist PI and/or research nurse coordinator in the planning and design of source documents for protocol.
• Assists in developing procedures for laboratory collection and storage.
• Assists in processing and shipping lab specimens; retrieves and/or sends identified research specimens certified if indicated as per regulations.
• Assists in precepting new clinical research staff and educating other research staff regarding scientific aspects of studies.
• Assists in processing and shipping lab specimens efficiently and cost effectively; maintains supply inventory and equipment; maintains regulatory standards.
• Assists with the budget development; may monitor ledgers.
• Adheres to internal controls established for department.
• May assist PI in obtaining Informed Consent from study participant and documents appropriately.
• Adheres to internal controls and reporting structure.

Requirements

• Bachelor's degree or equivalent.
• Two years of directly related experience in clinical research.
• Knowledge of Good Clinical Practice (GCP).

Nice-to-haves

• Experience in mentoring new staff.
• Familiarity with grant/protocol preparation and submission processes.

Benefits

• Equal Employment Opportunity policies promoting diversity and inclusion.