Scheduled Classes

Registration
View our scheduled dates to the right to register online or call 678-600-5649.

Description of Course
This training is designed to provide the participant with excellent hands on and practical knowledge to clinical research and the roles and responsibilities of Clinical Research Associates. This training will prepare or refresh your knowledge. As an added benefit training will be both observational and interactive. You will gain a complete knowledge of the 4 types of monitoring visits (PSV, SIV, IMV, and COV) as if you were shadowing a Certified Sr. CRA.

Who Should Attend

• Aspiring Clinical Research Coordinators
• Aspiring Clinical Research Associates – In-house or Field-based
• Aspiring Clinical Data Managers
• College Students
• Nurses
• New College Graduates – Any Discipline

You will learn

• The basics of organization and professionalism as a Clinical Research Associate
• Discuss & Demonstrate the important components of each type of monitoring visit
• Demonstrate knowledge of different study Phases and monitoring visits
• Demonstrate knowledge about Source Documents {including electronic}, Case Report Forms, Regulatory Binder, Study Drug Accountability, Laboratory & Supplies Accountability
• Understand the roles and responsibilities of the Clinical Research Associate , Investigator, Clinical Research Coordinator, and Clinical Research Data Manager
• Learn best practices regarding monitoring tools, travel arrangements and other useful tips