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Scheduled Classes

Registration
View our scheduled dates to the right to register online or call 1-(888)-988-3853.

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 Coordinators & Data Managers. 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 Senior Study Coordinator or Data Manager.

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 Coordinator/ Data Manager
• 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 study subject tools, and other useful tips