Clinical Research Associate / Coordinator program is Approved by New Jersey Department of Education and Department of Labor and Workforce, United States.
Recommended: Minimum - Bachelor 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.
Available as self paced training (PIP, pure internet program) Course Reading Material (chapters, PowerPoint presentations, Exercises, Quizzes & Final Exam).
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 a protocol development, assessment and reporting of adverse events and explains GCP-ICH guidelines along with other necessary regulatory information. The course emphasizes on 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 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 opportunity in clinical research field.
1) Upgrading the Knowledge required.
2) Better Resume Placement for promising jobs.
3) Low Investment, high learnings
4) Learn from Anywhere, Anytime at your pace.
5) Title Based learning.
Institutional Scholarship is available for selected on tuition. We review your education, certifications, and experiences (if applicable) to evaluate the eligibility and if found qualified an Institutional scholarship will be awarded on Tuition. Email us your resume to firstname.lastname@example.org to check on your eligibility. We will email you the details of the program along with eligible scholarship. Qtech’s objective is to provide you the right career pathway and advancement required to meet your goals.
The Post Training Assistance (PTA) program is provided to candidates who have completed Qtech-Sol Certification training program.
Our mission is to provide the best-in-class job oriented career development eLearning training courses and programs in clinical research.
Program is designed by industry experts for fresh graduates and professionals. The training provides in depth knowledge of roles and responsibilities of Clinical Research Associate.View details
Proceed to REGISTER for demo Access. Upon Login using your user-id and password, you will have access to first lesson for next 5 days.
It was 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.
The level and nature of participation was simply exceptional, concrete exercise, excellent analysis and feedback.The work assigned to interns are valuable and very useful. This CRA training is a value addition program, and helps me to face the global opportunities.
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.
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