Certificate Program in Clinical Research (CPCR)
This self-paced certificate course will provide you a comprehensive training on the concepts & processes in clinical research along with the application of GCP guidelines. This clinical research course will also train you for the entry-level job positions in clinical research (Clinical Research Coordinator, Trial Assistant etc.)
4.7 (1516 Ratings)
About the Course
With 250000+ clinical trials already registered at clinicaltrials.gov portal, the present worth of global clinical research industry is estimated to be more than $40B. ICH-GCP and regulatory guidelines provide a framework of principles which aims to ensure the safety of study subjects along with integrity and validity of data produced during trials. The industry offers a number of options for health science students & working professionals to excel their career as Clinical Research Coordinator, Trial Coordinator, Research Assistance, Trial Investigator, Research Nurse, Research Scientist etc.
Certificate Program in Clinical Research (CPCR) will provide you a comprehensive training on scientific, practical, ethical and technical concepts of the clinical trial along with the application of GCP guidelines. This 6 months course covers all the clinical research concepts and its applications in 13 modules covering 250+ topics. Each module is well explained in detail with the help of illustrations, examples, and flowcharts.
Who Should Enroll?
This course is specially designed for:
- Health-science candidates (Pharmacy, Life-Science, Medicine, AYUSH, Dental, Nursing, Physiotherapy, Ph.D. etc.) who are looking to gain knowledge & start their career in the clinical research industry.
- Fresher and experienced clinical research personnel.
Rs.7600 9500 20% Off
|20% Fee Discount: Till 28th Feb’18|
|Batch Starts: 28th February 2018|
|Learning: Online & Distance|
|Duration: 6 Months|
|Efforts: 60 Hours Approx.|
|Assessment: Single Exam|
|Includes: Certificate of Completion|
|Course Access: Lifetime|
Module 1: Introduction to Clinical Research
Module 2: Evolution of Ethics, Regulations & ICH-GCP
Module 3: Roles and Responsibilities of CR Personnel
Module 4: Clinical Study Process
Module 5: Institutional Review Board (IRB)
Module 6: Informed Consent Process
Module 7: Study Subject Recruitment & Retention
Module 8: Safety Reporting & Adverse Event Management
Module 9: Research Protocol
Module 10: Essential Research Documents
Module 11: Maintenance of Source Documents
Module 12: Site Closure
Module 13: Research Misconduct
Assessment and Evaluation through Exam
How This Works?
Upon enrollment, the course participant will get the course login details or course material before the start of batch via email.
Upon receipt of login details or material, the participant can read or log in to take the course modules anytime and from any device.
After reading all the course modules, the course participant is required to attempt and submit an exam.
Upon evaluation of exam, the certificate of completion will be issued to all the successful participants of the batch.
At the end of this course, you should be able to learn about the:
Concepts and processes involved in clinical research
Knowledge and skills required to start career in clinical research industry
GCP guidelines and its application in clinical trials
Roles & responsibilities of clinical trial personnel and stakeholders
Maintenance and management of clinical research documents
It is the best that one can have learning via online mode. Also, the response from the team was very prompt.Surubhi Rajan
This is a really good online learning site for clinical research professionals.Gautam Chawla
Overall experience of your website is very nice. Ease of handling material. Nice support staff.Kashish Ajmera
I feel Physis gives me immense knowledge about Clinical Research. Physis is excellent in quality of work and query resolution.Deepak Kaushik
I would like to take more courses such as Pharmacovigilance, but still needs some more time to think.Rakesh Sethi
It was a good experience to gain knowledge in the clinical research domain.Raja Biswas
Is it 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, exam, and certification of completion.
Do I have to take the course on specific timings?
There is no need to take the course module on particular timings. The course is self-paced and you can take the modules anytime.
Can I complete the course early also?
Yes, you can. In order to do so, you have to attempt and submit the online exam for evaluation.
I am a very 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 firstname.lastname@example.org
What is the difference between Online and Distance learning?
In online mode of learning, you will get login access to read the course modules. You can learn anytime and from any device. In distance mode of learning, you will receive a printed/ hard copy of course material at your corresponding address via post. So, you can choose any mode of learning as per your convenience.
How can I enroll and pay the fee?
To enroll and pay the course fee, follow the link STEPS TO ENROLL