Trauma Study Coordinator

Overview

Clinical Study Coordinators Helps with the logistical and administrative aspect of clinical trials and studies, ensuring adherence to protocols and regulatory requirements. Help facilitate participant recruitment, consent processes, and documentation management. Coordinate study visits, monitor adverse events, and maintain accurate records for successful study outcomes.

Job Summary

Clinical Study Coordinators Helps with the logistical and administrative aspect of clinical trials and studies, ensuring adherence to protocols and regulatory requirements. Help facilitate participant recruitment, consent processes, and documentation management. Coordinate study visits, monitor adverse events, and maintain accurate records for successful study outcomes.

• Clinical Study Coordinator, I — Supports logistical and administrative aspects of clinical trials; ensures adherence to protocols and regulatory requirements; facilitates participant recruitment, consent processes, and documentation management; coordinates study visits; monitors adverse events; maintains accurate records.
• Clinical Study Coordinator, II — Coordinates technical and administrative details in clinical trials with some supervision; assists Principal Investigators in achieving study objectives; reviews protocols; participates in recruitment and consent processes; maintains study documentation; coordinates resources; reports and tracks adverse events; completes and audits CRFs; assists with IRB documents; ensures proper specimen collection, processing, and shipment.
• Clinical Study Coordinator, III — Coordinates technical and administrative details; assists Principal Investigators; assesses protocol clarity and subject safety; reviews inclusion/exclusion criteria; participates in meetings; obtains informed consent, medical history, and demographics; coordinates facility and equipment availability; reports adverse events; manages protocol deviations and specimen handling; performs Clinical Research Assistant functions as needed.

• Equivalency statement: 1 year of higher education can be substituted for 1 year of directly related work experience (example: bachelor’s degree = 4 years of related experience).
• Clinical Study Coordinator, I:
  Requires a bachelor’s (or equivalency) + 2 years of directly related work experience or a master’s (or equivalency).
• Clinical Study Coordinator, II:
  Requires a bachelor’s (or equivalency) + 4 years or a master’s (or equivalency) + 2 years of directly related work experience.
• Clinical Study Coordinator, III:
  Requires a bachelor’s (or equivalency) + 6 years or a master’s (or equivalency) + 4 years of directly related work experience.

• A bachelor’s (or equivalency) with up to 2 years of directly related work experience or a master’s (or equivalency) degree; work equivalency accepted (1 year of higher education can be substituted for 1 year of related work experience).

• Requisition Number: PRN
  44016B
• Full Time or Part Time? Full Time
• Work Schedule
  
  Summary:
  
  M-F
• Department: 00269 - Orthopedic Surgery Operations
• Location:
  
  Campus
• Pay Rate Range: $45k - $58K
• Close Date: 4/12/2026
• Open Until Filled

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