Analysis Skills, Billing, Clinical Data Collection, Clinical Information Systems, Clinical Practices/Protocols, Clinical Research, Clinical Trial, Clinical Trial Management, Clinical Validation, Computer Skills, Data Management, Funding, IRB/IEC (Institutional Review Board/Independent Ethics Committee), Inventory Management, Microsoft Office, Operations Management, Presentation/Verbal Skills, Program Evaluation, Project Tracking, Record Keeping, Regulations, Research Protocols, Systems Administration/Management, Training/Teaching, Writing Skills
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.
- 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,
- 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.
- 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.
U
UT Health San Antonio School of Dentistry