Certificate Program for Clinical Research Associate (CRA)
Become A Certified Clinical Trial Monitor with this online and self-paced training program. This online CRA Certification course will train you to efficiently monitor & coordinate the day-to-day trial activities of a Clinical Trial Monitor in compliance with the applicable regulatory guidelines.
4.4 (500+ Ratings) 1950+ participants enrolled
About This Course
A Clinical Research Associate (CRA) or a Clinical Trial Monitor is primarily responsible to monitor, administrate, and supervise the overall progress of a trial. Effective clinical trial monitoring is essential to ensure smooth conduct and progress of clinical trial activities. This ultimately helps to generate quality research data for analysis and trial results.
If you are looking to start or advance your career as a CRA or you are already a Clinical Research Associate without any formal training, the course Certification for Clinical Research Associate” will certify and develop the skills to become a successful CRA.
CPCRA is an online & self-paced certificate program that will provide you comprehensive training on scientific, financial, practical, ethical, and technical concepts of clinical trial monitoring. This 10 weeks training course covers in-depth training for the role of clinical research associate (CRA) in 15 modules covering 150+ topics. Each module is well explained in detail with the help of illustrations, mock training, templates, examples, and flowcharts.
Who Should Enroll?
The course can be attended by:
Clinical Research Coordinators, Research Assistants, and Nurses looking to advance their career as Clinical Trial Monitor.
Newly appointed Clinical Research Associate (CRA)
Experienced CRAs interested in certification
Any researcher and healthcare professional who is looking to take the training & start their career as a Clinical Research Associate (CRA)
$240 $320 25% Off
Course Highlights
25% Early Bird Off until April 7
Last Date: April 25, 2025
Online and Self-paced Learning
Single Online Exam
Approx. 40 Hours of Effort
Global Acceptance
Course Curriculum
Module1: Introduction to Clinical Research
Module 2: Evolution of Ethics, Regulations & Guidelines
Module 3: Essential Clinical Trial Documents
Module 4: Investigator Site Selection & Assessment
Module 5: Development of Monitoring Plan
Module 6: Site Initiation, Documents Review & Delegation of Duties at Sites
Module 7: Clinical Trial Monitoring
Module 8: Inventory Planning & Tracking
Module 9: Source Document Verification (SDV)
Module 10: CRF Review, Collection & Coordination of Data Management
Module 11: SAE Review & Regulatory Compliance
Module 12: IP Accountability & Management
Module 13: Escalation, Prevention & Management of Violation/ Deviations
Module 14: Tracking of Enrolments, Payments & Ongoing Correspondence
Module 15: Site Closure
Assessment Through Mock Hands-On Training Online Exam
How Does This work?
You will get the course access details within 48 hours of enrollment.
After that, you can log in to take the course modules at your pace and timings from any device.
After finishing all the course modules, you have to attempt and submit an online exam. The exam is also self-paced.
After reviewing your exam, the certificate of completion will be issued to all the successful participants of the batch.
Learning Objectives
This course will help you to:
Develop required skills-set to effectively monitor and administer clinical trial sites.
Identify and define all the procedures to successfully plan, execute, monitor and control the activities of a trial.
Independently plan and execute global monitoring visits.
Learn the process of safety reporting requirements.
Identify, manage and report the trial deviations.
Effectively manage pre, during and after trial job functions in a time-bound manner.
Learners From Top Schools and Companies
To date, learners from 40+ countries and 105+ prestigious global schools and organizations are enrolled in this course.
Testimonials
Average Rating
I loved the mock hands-on training part of the clinical trial monitoring course. It was the first of its kind experience.
Covers enough content for beginners and the exam structure was very good.
I am new to research. CRC & CRA training has helped me to update my knowledge of clinical research.
The course modules were very easy to understand and the information is very well presented.
Great and very informative for all the researchers looking to advance their careers in clinical research.
I learned a lot from this course. It covers most of the aspects of clinical trial monitoring.
Top FAQs
Is this the entire course fee?
Yes, the fee mentioned above is the entire course fee and there is no additional fee attached to this course. The fee covers the cost of course modules, online exams and certification of completion.
Do I have to take the course at specific timings?
There is no need to take the course module at particular timings. The course is self-paced and you can take the modules anytime.
Can I complete the course early also?
Yes, you can. To do so, you have to attempt and submit the online exam for evaluation.
I am busy with my professional work/ studies. What if I don’t complete the course on time?
In this case, you can extend the timelines to complete the course. You can do so by dropping a request email in advance with your registered email id at info@physisglobalacademy.com
What if I don’t clear the exam?
Though the course modules are self-explanatory and you can comfortably clear the exam if you go through all the course modules. But in case you are unable to clear it in your first attempt then you will get a second (final chance) to attempt the exam.
How can I pay the fee?
To pay the course fee, follow the link STEPS TO ENROLL or you transfer the applicable course fee directly through your PayPal account to our PayPal account at info@physisglobalacademy.com
Interested in group enrollment?
Get up to a 50% discount when you sign up for our plans customized for individuals and companies.
You Might Also Be Interested In
Certificate Program in Clinical Trial Project Management
Certificate Program for Clinical Research Coordinator (CRC)
Certificate Program in Medical Writing of Clinical Trial Documents
