Certificate Program in Clinical Research
The clinical research certificate course will provide you comprehensive training on the concepts & processes of clinical trials along with the application of ICH GCP guidelines. This training course will also train you for entry-level job positions in the clinical research industry (Clinical Research Coordinator, Trial Coordinator, Trial Assistant, Clinical Research Nurse etc.)
4.6 (1150+ Ratings)
About This Course
Clinical research is a branch of healthcare science that determines the safety and effectiveness of medications, devices, diagnostic products and treatment regimens intended for human use.
To date, more than 375000 clinical trials are registered at clinicaltrials.gov. The present estimated worth of the global clinical trial industry is 44.3 billion. ICH-GCP and regulatory guidelines provide a framework of principles that aims to ensure the safety of study subjects along with integrity and validity of data produced during trials. The industry offers several career options for health science professionals to advance their career for the job positions of Clinical Research Coordinator, Trial Coordinator, Research Assistance, Trial Investigator, Research Nurse, Research Scientist etc.
If you are looking to start your career in clinical research or you are already in this industry without any formal training, the course “Certificate Program in Clinical Research” will certify and guide you to develop the required skills.
The 13 in-depth course modules of Clinical Research diploma course will train you to efficiently manage & coordinate the day-to-day trial activities of a study in compliance with applicable regulatory guidelines. Each module is well explained in detail with the help of illustrations, examples, and flowcharts.
Who Should Enroll?
The course can be attended by:
Health-science professional (working/fresher/ student) from Pharmacy, Life-Science/ Biotech, Medicine, AYUSH (Alternate Medicine), Dental, Nursing, Physiotherapy, Ph.D. background who are looking to gain knowledge & start their career in the clinical research industry.
Fresher and experienced clinical trial personnel
Other specialists from Medical Affairs, Pharmacovigilance, Pharmaceutical Development Scientists, Translational Medicine, Regulatory Affairs etc.
Rs.7600 9500 20% Off
Course Highlights
20% Discount Until 15th March
Last Day to Enroll: 31st March 2025
Online and Distance
Rs. 7600 / $120 After Discount
6 Months Duration
Single Online Exam
Global Acceptance
Approx. 50 Hours of Effort
Benefits After Enrollment
JOB ORIENTED CURRICULUM
Our course modules covers all the elements required to impart skills & knowledge to get a relevant job in the industry.
GLOBALLY VALID CERTIFICATE
Our course modules are based on ICH-GCP and applicable regulatory guidelines which are valid globally. So, The certificate is acceptable across the industry.
PLACEMENT ASSISTANCE
Upon course completion we help you with placements through our referrals and industry experts for the relevant job positions.
RESUME & INTERVIEW
Along with placements, we also assist you to prepare your resume as per the industry standards along with interview preparation.
Enroll & Get A Free Beautifully Designed Resume
You Have Less Than 6 Seconds to Impress the Employer.
When you enroll in a course, we transform your dull-looking CV into a “beautiful & professional CV” to make it stand out from the rest for free of cost.
We help our course participants to redesign their CV/ resume as per industry standards. This amplifies their chance to get selected for the relevant job positions.
Course Curriculum
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.
Learning Objectives
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 a career in the clinical research industry
GCP guidelines and their application in clinical trials
Roles & responsibilities of clinical trial personnel and stakeholders
Maintenance and management of clinical research documents
Testimonials
Average Rating
Top FAQs
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 info@physislearningacademy.com
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
Training for Team or Want to Enroll in Multiple Courses?
Choose a plan and save more on courses.
You Might Also Be Interested In
Certificate Program in Pharmacovigilance
Certificate Program in Drug Regulatory Affairs (DRA)
Certificate Program in Medical Writing
