Description:

The CCRC (Certified Clinical Research Coordinator) course is designed to provide participants with the necessary knowledge and skills to work as a clinical research coordinator in the healthcare industry. This course covers the fundamental concepts of clinical research coordination, including the responsibilities and duties of a coordinator in managing clinical trials and ensuring compliance with regulatory requirements.

Key Highlights:

• Learn key concepts and principles of clinical research coordination
• Understand the role and responsibilities of a research coordinator
• Gain practical skills in managing clinical trials and ensuring compliance
• Explore ethical considerations and regulatory requirements in clinical research
• Prepare for the CCRC certification exam

What you will learn:

• Learning Outcome 1
  Understand the basics of clinical research coordination and its importance in the healthcare industry.
• Learning Outcome 2
  Learn how to effectively manage clinical trials, including participant recruitment, data collection, and documentation.
• Learning Outcome 3
  Explore the ethical considerations and regulatory requirements involved in conducting clinical research.
• Learning Outcome 4
  Develop proficiency in maintaining accurate records, ensuring participant safety, and adhering to Good Clinical Practice (GCP) guidelines.
• Learning Outcome 5
  Prepare for the CCRC certification exam by reviewing the exam content and practicing sample questions.