Online Clinical Research Course - Part- 2 | Your Complete Beginner to Advanced course

Online Clinical Research Course - Master the Clinical Research, Ethics, ICH GCP, Routine Monitoring Visits, Monitoring of Trials, Investigational Drug Management.

Beginner 5(16 Ratings) 99 Students enrolled English
Created by Vaishali Deshpande
Last updated Mon, 01-Apr-2024
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Course overview

You want to upgrade your skills and start career in ever growing clinical research industry then this course is perfect for you!

Start learning Clinical Research to start your career in most growing field of Pharma & life-Science Industry!

Either you're completely brand new to Clinical Research, or you've played around it but want to get more comfortable with Clinical Research. Either way, this course will be great for you.

Clinical Research is the #1 field of Pharma & life-Science Industry. This full course is the best way to learn how to implement it.

What makes me qualified to teach you?

My name is Mrs Deshpande and I've been in the Clinical Research for over a Two decade. Plus I'm the creator of some of the most popular online courses - with over 2000+ students like these ones:

Awesome course, easy to follow! – Radha Jaiswal

Your course is amazing, so I can say that I am learning a lot. Your English is very easy to understand ( I'm from Brazil). Thanks for sharing your amazing knowledge. – Santosh Chame

My Promise to You

I'll be here for you every step of the way. If you have any questions about the course content or anything related to this topic, you can always post a question in the course or send me a direct message. 

I want to make this the best course on Clinical Research. So if there is any way I can improve this course, just tell me and I'll make it happen.

What is this Clinical Research course all about?

In this complete guide to Clinical Research, you'll not only learn all of the topics and segments of Clinical Research, but also how to implement in real Industry so that you can crack any interview and start your career with a bang.

This course will cover everything you need to know to start your career, including:

<!--[if !supportLists]-->·         <!--[endif]-->Basics in Clinical Research

<!--[if !supportLists]-->·         <!--[endif]-->Drug Development Process

<!--[if !supportLists]-->·         <!--[endif]-->Good Clinical Practice (GCP) – ICH E6

<!--[if !supportLists]-->·         <!--[endif]-->Protocol Designing

<!--[if !supportLists]-->·         <!--[endif]-->Drug Regulatory Affairs (Clinical Trial)

<!--[if !supportLists]-->·         <!--[endif]-->Clinical Safety and Pharmacovigilance

<!--[if !supportLists]-->·         <!--[endif]-->Monitoring of Clinical Trials

<!--[if !supportLists]-->·         <!--[endif]-->Clinical Data Management

By the end of this course, your confidence as a Clinical Researcher  will soar. You'll have a thorough understanding of Clinical Research  domain for fun or as a career opportunity.

Go ahead and click the enroll button, and I'll see you in lesson 1!

What will i learn?

  • Knowledge of clinical research industry
  • Basics of Clinical Research and its Terminologies
  • What is the career pathway in Clinical Research
  • In depth study of how clinical trial are conducted along with some case studies.
  • Will be gaining profound knowledge of informed consent
  • Clinical Data Management
  • You will be job ready for clinical research domain
  • Stake holders of Clinical Research
  • Process of drug development and understand different clinical trials phases
  • Detail study of Good Clinical Practices
  • Will look at the purpose of essential document requirements
Requirements
  • Ideally who has completed their graduation in science, pharmacy or ailed branch also who are interested in medicine field
Curriculum for this course
45 Lessons 09:31:43 Hours
Monitoring of Trials
7 Lessons 02:24:20 Hours
  • Audits and Inspections
    00:25:36
  • Flow of Events
    00:36:45
  • Investigational Drug Management
    00:26:37
  • Routine Monitoring Visits
    00:34:50
  • Site Visit Flow
    00:20:32
  • Monitoring of Trials- Notes
    .
  • Monitoring of Trials- Quiz
    00:00:00
Regulation
13 Lessons 02:41:50 Hours
  • Application of Permission
    00:15:29
  • Approval of Clinical Trial
    00:13:13
  • CDSCO
    00:16:30
  • Code of Federal Regulation (CFR)
    00:15:10
  • CT_Rules_2019
    00:30:06
  • ICMR Guidelines
    00:48:03
  • Medical Devices
    00:23:19
  • Indian Medical Devices
    .
  • DoH Oct 2013
    .
  • Guidelines for Industry
    .
  • References
    .
  • The Belmont Report
    .
  • Regulation- Quiz
    00:00:00
Safety Reporting
16 Lessons 02:24:08 Hours
  • AE_SAE Reporting Process
    00:15:34
  • Adverse Event Reporting
    00:22:38
  • Recording of Event
    00:11:15
  • Medical Management of Adverse Events
    00:09:43
  • Handling Death
    00:04:22
  • Unblinding of Drug
    00:02:47
  • Clinical Safety and Pharmacovigilance
    00:24:38
  • E2A- Clinical Safety and Data Management
    .
  • Media 436
    .
  • Naranjo Assessment
    .
  • Order and Formulate to Determine the Quantum
    .
  • SAE Reporting
    .
  • Introduction to Aggregate Reporting
    00:07:27
  • Medical Assessment -2
    00:30:15
  • Medical Assessment -1
    00:15:29
  • Safety Reporting- Quiz
    00:00:00
Clinical Data Management
9 Lessons 02:01:25 Hours
  • CDM- 21 CFR Part 11
    00:15:15
  • CRF_Design_2
    00:26:16
  • Introduction to CDM
    00:10:44
  • Data Entry Methods
    00:15:19
  • Query Management
    00:20:14
  • Source data validation
    00:26:29
  • Future of Data Management
    00:07:08
  • Clinical Data Management- Notes
    .
  • Clinical Data Management- Quiz
    00:00:00
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About instructor

Vaishali Deshpande

90 Reviews | 780 Students | 15 Courses
Student feedback
5
16 Reviews
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Reviews

  • Vedant Chikate
    The course really helped me understand the basics to advanced clinical research!
  • Aishwarya Sancheti
  • Radha Mhapankar
    Very good content - crisp, concise and easy to understand. Thanks to Vaishali ma'am for all the guidance and support.
  • Abhay Mahajan
  • Pooja Thanki
  • Prasun Chakraborty
  • Yugandhara Kulkarni
    Nice experience.
  • Sanket Khule
  • Shobhana Jadhav
  • Samiksha Wadekar
  • Amol Kokare
  • Gaurav Telang
  • Sonali Zanjurne
  • Shubhada Borale
  • Rutuja Patil
    Thanks to TechnoBridge Systems, I secured a placement at Fortrea CRO for a Pharmacovigilance case processing role. All thanks to the excellent training provided by my mentor. Following the completion of my Clinical Research Course, the supportive placement team made it all possible.Support placement team is very active.The sessions explained in simple and easy manner so they are understandable.I recommend TechnoBridge to anyone looking to start their career in Clinical Research. Grateful for TechnoBridge's guidance.
  • Pallavi Jadhav
22000 Rs 15000 Rs
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