Post Graduate Diploma in Clinical Research Part 2

Join the best Clinical Research Course with 100% Placement Assistance & Learn clinical research, pharmacovigilance, clinical data management, medical writing & etc.

Advanced 0(0 Ratings) 0 Students enrolled English
Created by kunal Narhare
Last updated Mon, 12-Aug-2024
+ View more
Course overview

About Clinical Research Course:

Clinical research investigates the safety and effectiveness of medications, devices, diagnostics, and treatment plans for various health conditions, including prevention, treatment, diagnosis, and symptom relief. This exciting field lies at the heart of medical advancements, and our Clinical Research course equips you with the knowledge and skills to become a vital part of it.

TechnoBridge Systems provides best live online clinical research course with 100% placement assistance in India. Our regulatory affairs diploma syllabus designed by 27+ years experienced industry experts in that we cover all the important aspects like Clinical Research, GCP-IC E6, Clinical Data Management, Drug Development Process, Pharmacovigilance, Regulatory Affairs, Monitoring of Trials, & Protocol Designing. 

Course Objectives:

  • Master the fundamentals of clinical research, from study design to data analysis.
  • Understand the drug development process from pre-clinical testing to market approval.
  • Gain expertise in Good Clinical Practice (GCP) and international regulatory guidelines.
  • Develop skills in managing clinical trial data, including collection, analysis, and reporting.
  • Identify and report adverse events with proficiency in pharmacovigilance practices.
  • Learn the intricacies of protocol design and monitoring clinical trials effectively.
  • Enhance your employability skills with resume writing, interview preparation, and job placement assistance.

How to Enroll in Clinical Research Course?

Start your journey into clinical research with just a few clicks! Simply visit our website and click the "Register Now" button on the course page. Fill out the application form, and our friendly team will be in touch to guide you through the process.

Clinical Research Course Eligibility

This course welcomes individuals with a passion for research and a life science background. We cater to any life science graduates like B.Sc./M.Sc. (Biology, Microbiology, Nursing) BPharm/M.Pharm, and allied disciplines. No prior experience in clinical research is required, but a strong foundation in science and analytical skills is beneficial.

Clinical Research Course Fee Structure:

We believe education should be accessible to everyone. Therefore, we offer flexible fee structures to suit your needs:

  1. For one-time payment our clinical research fees is 22000/-
  2. For payment in 2 installment our clinical research fees is 25000/-

Course Methodology:

Our immersive learning approach ensures you get the most out of your studies:

  • Live online & Pre-Recorded Sessions: Learn from industry experts through interactive lectures and engaging discussions.
  • Case studies and assignments: Apply your knowledge to real-world scenarios and hone your practical skills.
  • Mock interviews: Gain confidence and prepare for job interviews with personalized feedback.
  • Unlimited placement support: Benefit from our dedicated placement team that connects you with top companies in the field.

Course Syllabus:

The curriculum is meticulously designed to cover all aspects of clinical research:

  • Module 1: Introduction to Clinical Research
  • Module 2: Drug Development Process
  • Module 3: Good Clinical Practice (GCP)-ICH E6
  • Module 4: Clinical Data Management
  • Module 5: Pharmacovigilance
  • Module 6: Regulatory Affairs
  • Module 7: Monitoring of Trials
  • Module 8: Protocol Designing
  • Module 9: Advanced Topics in Clinical Research
  • Module 10: Career Guidance & Placement Assistance

Why Choose TechnoBridge for Online Clinical Research Course?

  • 27+ Years Exp. faculty: Learn from industry experts with practical experience and a passion for teaching.
  • Comprehensive curriculum: Master all aspects of clinical research from theory to practical application.
  • Interactive learning environment: Engage in live sessions, discussions, and practical exercises to solidify your understanding.
  • Career-focused guidance: Get personalized assistance with resume writing, interview preparation, and job placement.
  • Affordable and flexible fee structure: Choose from various payment options to fit your budget.
  • Lifetime access to course materials: Continue learning and revisiting key concepts even after course completion.

Career Opportunities:

The clinical research field offers a plethora of exciting and well-paying careers. With our comprehensive training, you can pursue fulfilling roles in diverse areas, including:

  • Clinical research associate (CRA)
  • Clinical data manager
  • Pharmacovigilance specialist
  • Medical writer
  • Project manager

Type of companies hiring CR professionals:

  • Pharmaceutical companies
  • Biotechnology companies
  • Contract research organizations (CROs)
  • Medical device companies
  • Government agencies
  • Academic research institutions

What will i learn?

  • Knowledge of clinical research industry
  • You will be job ready for clinical research domain
  • Basics of Clinical Research and its Terminologies
  • Stake holders of Clinical Research
  • What is the career pathway in Clinical Research
  • Process of drug development and understand different clinical trials phases
  • In depth study of how clinical trial are conducted along with some case studies.
  • Detail study of Good Clinical Practices
  • Will be gaining profound knowledge of informed consent
  • Will look at the purpose of essential document requirements
  • Clinical Data Management
Requirements
  • Ideally who has completed their graduation in science, pharmacy or ailed branch also who are interested in medicine field
Curriculum for this course
20 Lessons 08:36:45 Hours
Monitoring of Trials
5 Lessons 02:19:27 Hours
  • Difference Between Monitoring, Audit & Inspection
    00:17:31
  • Flow Of The Event
    00:29:41
  • Monitoring Process
    00:54:21
  • Investigational Product Accountability (IPA)
    00:24:01
  • Site Visit Flow
    00:13:53
Regulation
5 Lessons 02:55:03 Hours
  • Application for Permission and Approval of Clinical Trials
    00:15:29
  • ICMR Guidelines in Clinical Trials
    00:25:27
  • Medical Device Regulation MDR 2017
    00:14:02
  • New Drugs and CT Rules 2019
    01:26:43
  • Regulatory Authoeities in India(CDSCO)
    00:33:22
Safety Reporting
4 Lessons 01:55:05 Hours
  • ADR Classification and Evolution
    00:39:20
  • Adverse Event Reporting in Clinical Trials
    00:38:05
  • Periodic Safety Update Reports PSURs
    00:12:24
  • Pharmacovigilance and its Aims
    00:25:16
Clinical Data Management
6 Lessons 01:27:10 Hours
  • Code of Federal Regulations (CFR) 21 CFR PART 11
    00:10:31
  • CRF Design
    00:18:52
  • Data Entry Methods
    00:13:58
  • Introduction to Clinical Data Management (CDM)
    00:14:00
  • Query Management
    00:17:23
  • Quality Control and Quality Assurance in Clinical Trials
    00:12:26
+ View more
Other related courses
16:10:25 Hours
5 1158 35000 Rs 27000 Rs
14:10:15 Hours
5 1158 37000 Rs 27000 Rs
06:38:42 Hours
5 1158 22000 Rs 16000 Rs
09:31:43 Hours
5 1158 22000 Rs 16000 Rs
08:55:39 Hours
5 1158 30000 Rs 25000 Rs
About instructor

kunal Narhare

6 Reviews | 18 Students | 9 Courses
Student feedback
0
0 Reviews
  • (0)
  • (0)
  • (0)
  • (0)
  • (0)

Reviews

20000 Rs 16000 Rs
Includes:
Quick Enquiry