Certification Training for Clinical Research Associate (CRA)
Become a Certified CRA with Online CRA Certification Course. CRA Certificate program will provide you training and skills on the roles & responsibilities of a Clinical Trial Monitor required before, during and after clinical trials. CRA Certification will also prepare you for the profile of Clinical Trial Monitor/ Clinical Research Associate
4.4 Average Rating (1400+ Course Participants)
$192 $240
20% Fee Discount Until April 30
April 2024 Batch
Last Date of Application: April 30, 2024
Online & Self-Paced
Approx 50 Hrs. of Efforts Required
Course Overview
The success of a clinical trial largely depends on the quality of clinical trial data generated during the study and a Clinical Research Associate (CRA) has the prime responsibility to monitor the data.
“A Clinical Research Associate (CRA), also called Clinical Trial Monitor is a health-care professional who is primarily responsible for monitoring, coordinating, supervising, and managing the overall progress of a clinical trial in a GCP compliant fashion.”
The online course “Certification Training for Clinical Research Associate (CTCRA)” would provide you an in-depth knowledge of all the roles and responsibilities undertaken by a CRA during a clinical study. Check the complete Course Curriculum.
CRA Training Program will make aspirants and working professionals to prepare them for the role of Clinical Trial Monitor.
Course Features
Course Fee: $192 (20% Discount)
Batch: April 2024
Last Date: April 30, 2024
Course Duration: 12 weeks
Certificate Validity: Global
Timings: Self-Paced
Mode of Learning: Online
Exam: Single, Online
Efforts: Approx 50 Hours
Content Access: Lifetime
Language: English
Includes: Exam Fee and Certificate of Completion
Course Curriculum
Clinical Research Associate Training syllabus covers the following course modules:
Module 1: Introduction to Clinical Research
Module 2: Evolution of Ethical Research principals, Regulations and Guidelines
Module 3: Essential Clinical Trial Documents
Module 4: Investigator Site Selection and Assessment
Module 5: Development of Monitoring Plan
Module 6: Site Initiation, Review of Trial Documents & Delegation of Duties at Individual Site
Module 7: Clinical Trial Monitoring
Module 8: Inventory Planning and Tracking
Module 9: Source Document Verification (SDV)
Module 10: CRF Review, Collection & Coordination of Data Management Activities
Module 11: Serious Adverse Event (SAE) Review & Regulatory Compliance
Module 12: Investigational Product (IP) Accountability & Management
Module 13: Escalation, Prevention & Management of Violation/ Deviations
Module 14: Tracking of Enrollments, Payments & Ongoing Correspondence
Module 15: Site Closure
Assessment through Self-paced Online Exam
Learner’s Profile
This online Clinical Research Associate (CRA) Training course caters to global health science working professionals, masters and graduates from international medical and healthcare universities, CROs and healthcare companies.
Schools, Universities and Companies
Happy Learners
SCSU, USA
Coordinator, University of Rochester, USA
Hong Kong
Research Medical Assistant, USA
Baylor College of Medicine, USA
Data Manager, ASL Toscana Nord Ovest, Italy
Course Eligibility
- Clinical Research Professionals
- Aspirants (graduates, masters, PhD and working professionals) from health science background: Pharmacy, Medicine, Dental, Nursing, Public Health, Life-Science, Biotechnology, Physiotherapist, Traditional/ Alternative Medicine etc.
Enrollment Process
The enrollment process consists of 3 simple steps to enroll in the course.
STEP 1: ADD TO CART
Click Enroll Now Button, Add the course to your cart, click View Cart Button and Proceed to the checkout page.
STEP 2: FILL THE DETAILS
Fill your personal and billing details on the checkout page, Check T&C Box and Click Pay Now Button
STEP 3: PAY THE FEE
Pay the course fee securely via PayPal with your Card or Net Banking & get immediate access to the course.
To know step by step process visit the Page HOW TO ENROLL
Course Benefits
- 15 online self-paced learning modules (approx. 50 hrs. of learning).
- A self-paced online exam for your assessment.
- Certificate of Completion and a Performance Sheet on successfully completing the course.
- Opportunity to explore a career in Clinical Research Operations as Clinical Research Associate.
Interested to enroll in 2 or more courses?
Save more with our Course Plans made for individuals and teams.
Top FAQs
When will I get the course access after paying the fee?
It generally takes up to 48 hours to email you the course login credentials.
Can I complete the course earlier than 12 weeks?
Yes, you can.
How the course modules will be delivered to me?
You can access our e-learning portal. You have to log in with your Username and Password via email.
I am a busy working professional, can I take this course?
Yes, more than 80% of course participants are working. The course modules are completely self-paced. So, you can finish the course at your pace and time.
I am a student at present; can I take this course along with my studies?
Yes, you can take this course along with your regular studies.
Are there any specific timings to take the course modules?
No, the modules are self-paced. You can learn the module as per your convenient timings.
How the examination will be conducted?
Once you are through with course modules and want to take the examination, you just need to drop us an email to get the exam access.
Request to take the online exam can be forwarded at any point in time.
When will I receive the Certificate and Performance Sheet?
We generally take up to 14 working days to evaluate you and issue a Certificate of Completion with Performance Sheet after submission of your exam.
How the certificate will be delivered to me?
A print-ready Certificate of Completion will be issued through email upon successful completion.
Can I pay the fee in installments?
Yes, you can pay the fee in maximum of 2 installments. To pay the fee in installments, you need to contact us at admin@dnasysacademy.com
You can also check our FAQs Page for further queries.
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