CCRP exam Test Prep

Clinical Research Associate Exam Test-Prep

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Description

This intensive program is designed to equip aspiring CRAs with the knowledge, skills, and confidence needed to excel in the dynamic field of clinical research. I leveraged up-to-date research and ongoing discussions regarding FDA rules and regulations, making use of easily accessible FDA and federal laws that are available online. I conveyed all information through video presentations in, concise downloadable notes, and high order thinking questions in English.

The course encompasses:

  1. Fundamentals of Clinical Research: Gain a solid foundation in the principles and regulations governing clinical research, including Good Clinical Practice (GCP) guidelines.

  2. Clinical Trial Management: Learn the end-to-end process of planning, conducting, monitoring, and reporting on clinical trials.

  3. Ethical and Regulatory Compliance: Explore the ethical considerations and regulatory requirements that govern human subject research.

  4. Quality Assurance and Auditing: Understand how to maintain the highest standards of quality and compliance within clinical research projects.

  5. Risk Assessment and Mitigation: Identify potential risks in clinical trials and develop strategies to mitigate them effectively.

  6. Protocol and Investigator Interaction: Learn to collaborate with investigators and research teams to ensure study success.

  7. Exam Readiness: Benefit from practice exams, quizzes, and real-world case studies to enhance your exam preparedness.

Upon completing this course, you'll be well-prepared to tackle the Clinical Research Associate certification exam with confidence. Join us and take the first step towards a rewarding career in clinical research. Your future as a CRA starts here!

What You Will Learn!

  • Ethical principals guiding clinical research and regulatory requirements of IRB related to research study start up, implementation and closure
  • 4 weeks
  • Critically think over protocols.
  • Review research protocols with me to apply principles learnt in the course.
  • Define the roles and responsibilities of IRB, FDA, sponsors, and investigators along with overseeing the overall operational workflow.

Who Should Attend!

  • Aspiring Clinical Research Associates, students volunteering in research, journal reviewers and editors.
  • People with brief professional experience in clinical research looking to expand their horizon and find out what lies beyond the barrier.