Clinical Research - Role based Projects (CRAP) - Qtech-USA is a Clinical Science training provider as Private Career School offering Job focused training for Clinical Research, Drug Safety, Pharmacovigilance, CDM , Healthcare and SAS Programming

This program is approved by New Jersey Department of Education (DOE) and Department of Labor and Workforce Development (DOL). Funding Option is available to qualified NJ Resident students, contact us to check on requirements.

The course provides a thorough Foundation, Advanced and Project Management related concepts focusing clinical trials, drug development, Study design, Project Management, and Monitoring concepts of Clinical Sciences in reference to roles and responsibilities performed by Clinical Research Associate. The concepts include protocol development, assessment and reporting of adverse events and explain GCP-ICH guidelines along with other necessary regulatory information. The course emphasizes on the understanding of the science and the expectations of initiating, conducting, monitoring, and managing clinical trial-related work. This training will develop the technical skills and knowledge pertaining to the roles and responsibilities of CRA – In House. Students will get exposure to real-time practices pertaining to Case Report forms (CRFs), Trial Master File (TMF), Clinical Trial Protocol, Clinical Trial Budget, and Audit. The course curriculum is designed to give an edge to obtain job opportunities in the clinical research field.

Our Programs are delivered in 2 Different ways for convenience of student:


  • Self-Paced Individual Program (SIP)
    – Skill and Job Oriented Certificate programs, delivered as Self-Paced Online with project solutions.

  • Self-Paced Blended Program (SBP)
    – Skill and Job Oriented Certificate programs, delivered as Self-Paced Online with project solutions. Support thru Email and Phone for queries. Student participates in 7 days Post Training Assistance program for Resume preperation.
  • Admission Requirements:

    Recommended: An Associate or Bachelor’s degree in Medicine, Nursing, Pharmacy, Public health Biology, Biochemistry, Biotechnology, Chemistry, Clinical Research, Biomedical Engineering, Public health, Pharmacology, or toxicology, Medical Device & Technology, Psychology, Sociology and Healthcare Administration.

  • Institutional Scholarship / Promotion:

    Institutional Scholarship / Promotion is available for selected on tuition. We review your educational background, certifications, and prior experiences (if applicable), to evaluate your eligibility. The qualified student will be provided with the promo code for scholarship on Tuition.

    Please Email your resume to Human Resources qpdc@qtech-solutions.us to check on your eligibility. We will contact you. Qtech’s objective is to provide you the right career pathway and advancement required to meet your career goals.

  • Learning Outcomes:
    The Benefit Student Gains
    • Upgrading the Knowledge required.
    • Better Resume Placement for promising jobs.
    • Low Investment, high learnings
    • Learn from Anywhere, Anytime at your pace.
    • Job and Title Based Tasks as followed and Practiced in industry
    • Applying Concept into Real-time (Policies, governance and tools)
    • Work on Role Based Tasks followed and Practiced in industry
    • Mocks and Narratives for Client Discussions
    • Readiness to work with limited support

    LISTED AS PRIVATE SCHOOL (USA)

  • Career Pathways

    Our objective is to help students to meet the following career pathways. Typical Clinical Research Associate (CRA) Job Titles the candidates can apply after this training program are:

CLINICAL RESEARCH JOB TITLES

Our objective is to help students to meet the following career pathways. Typical Clinical Research Associate (CRA) Job Titles the candidates can apply after this training program are:

Curriculum Overview

Program is designed by industry experts meeting job and title-based learnings needed for students and young professionals to get into jobs. The training provides in depth knowledge of roles and responsibilities of Clinical Research Associate/ Clinical Research Coordinator. The curriculum includes theoretical and practical aspect of the role and tasks performed on day-to-day basis, along with exposure to various exercises per industry requirements.

Clinical Research – Role based Projects (CRAP)
LIST OF TOPICS

1. Introduction to Clinical Trials

2. FDA Regulations

3. Institutional Review Board(IRB)

4. IRB Regulatory Correspondence

5. Protocol Design and Development

6. Protocol

7. IND Application

8. Informed Consent Preparation

9. Informed Consent Form

10. CRF Design and Data Capture

11. Case Report Form (CRF)

12. Investigator Selection

13. Investigator Meetings and Timelines

14. Study Initiation

15. Site Monitoring

16. Co-Monitoring Visits

17. Study Initiation Visit

18. Pre-Study Site Visit (PSSV)

19. Clinical Trial Budget

20. Introduction to Adverse Event Reporting and Classification

21. Trial Master File (TMF)

22. CTMS Track Recording

23. Database Lock

24. Clinical Trial on Site Audit

25. Audit

Reviews

  • Qtech Solutions Inc. has provided me with the education needed to work as a Clinical Research Associate. The program was extremely helpful and the instructions were very knowledgeable.

    Maureen D (Texas)

  • It was a very interesting CRA training course. Topic, professional presentation, Quiz and test, makes the difference between a good training session and a GREAT training session. I like the competent materials course.

    Gamal A (New Jersey)

  • The level and nature of participation was simply exceptional, concrete exercise, excellent analysis and feedback. The work assigned to interns is valuable and very useful. This CRA training is a value addition program and helps me to face the global opportunities.

    Sangeetha T (Texas)

  • Category:
    Clinical Research
  • Duration:
    08 Weeks
  • Price:
  • Language:
    English