All About Clinical Research (Part A)

Introduction to Clinical Research and ICH/GCP

Course Overview

This training is designed to provide the participant with an excellent introduction to clinical research and the roles and responsibilities of Clinical Research Associates, Clinical Research Coordinators, and Data Managers. It will explore topics and hands-on knowledge relevant to those considering a career as an entry-level monitor, site coordinator, or data manager. Additionally, this course is appropriate for individuals seeking a new career or career change, but do not know which job track within clinical research to pursue.

Who Should Attend This Course?

  • Aspiring Clinical Research Coordinators

  • Aspiring Clinical Research Associates

    In house or Field Based

  • Aspiring Clinical Data Managers

  • Aspiring Regulatory Specialists/Coordinators

  • Currenet College Students

  • New College Graduates

    Any Discipline

  • Nurses

    RN's. BSN's, LPN's & Nurse Practitioners

  • Doctors

    MD, PhD, Pharm D, DO, PA

  • Newly Hired Study Coordinators, Clinical Research Associates and Regulatory Coordinators

Pre-requisite

No pre-requisites. This is an entry-level course

You Will Learn To:
Discuss the History of Clinical Research
Discuss the Federal Code of Regulations and ICH/Good Clinical Practices Guidelines
Define the Informed Consent Process
Understand the Roles and Responsibilities of the Clinical Research Associate
Understand the Roles and Responsibilities of the Clinical Research Coordinator
Understand the Roles and Responsibilities of the Clinical Research Data Manager
Understand the Roles and Responsibilities of the Regulatory Coordinator

Are You Ready to Learn More About Clinical Research?

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