Comprehensive Clinical Research Training

Highlights

The Comprehensive Clinical Research Training is designed to provide training and education for Investigators, Research Nurses, Clinical Research Coordinators and other research staff who conduct human subjects research. The program focuses on standards and techniques for conducting efficient, effective, and compliant clinical research. Regardless of the amount of research experience, investigators, coordinators and other key research staff will benefit from updates on current federal regulations, best practices, and available resources.

Objectives

Provide an overview of the research infrastructure and institutional resources
Provide training in accordance with Good Clinical Practices for investigator-initiated, industry-sponsored, and grant-funded clinical research in context to the Clinical Research Study Lifecycle.
Implement practical methods to manage clinical research projects and conduct research activities efficiently and effectively.
Train to the highest standards of practice and regulatory requirements for critical job functions of the Investigator and research staff.
Offer practical suggestions, tips, and resources for fulfilling Investigator and research staff job functions.

Training Sessions

The training consists of four (4) two-hour sessions once a week over the course of a month. Registration for training is required. A certificate of completion is provided after attending all four sessions.

Session 1