Job Description

Under limited supervision, responsible for assisting with the administration, organization and implementation of trial operations, systems management, and training/education. Provides specialized and technical reviews of clinical trial research protocols, funding agreements and billing processes.

Responsibilities

• Administers, organizes and conducts training/educational programs in connection with clinical trial operations, systems and management.
• Maintains records of training activities, progress, and program effectiveness.
• Ensures distribution and maintains inventory required for execution of research protocol(s).
• Assists in the determination of guidelines for new protocols.
• Collects and prepares data for various clinical trial related reports.
• Compiles reports, documents and correspondence for regulatory agencies, participating clinical trial sites and internal departments to monitor and evaluate progress.
• Develops, coordinates and conducts training in collaboration with clinical trial subject matter experts.
• Serves as liaison between clinical trial management systems end users and management systems support team.
• Performs all other duties as assigned.

Qualifications

• Knowledge of scientific concepts related to the design and analysis of clinical trials.
• Knowledge of data collection and management methodologies of clinical trial.
• Ability to demonstrate excellent written and verbal communication.
• Proficiency with computers, including Microsoft Office.

EDUCATION:

Bachelor's Degree degree in related field is required.

PREFERRED:

IRB experience, regulatory affairs experience, and clinical trials experience

This position may require the ability to maintain the security and integrity of UT San Antonio and its infrastructure per Texas EO-GA-48.

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