Understanding the Basics of Clinical Trial Protocol (Part 1)

In this video we explain the basics of Clinical Trial Protocol and understand Protocol Design, Study design, Data managements plan, Participant selection among many aspects of clinical trial protocol.
#protocol #trials #clinicalresearch #datamanagement #design #clinicalresearchassociate #clinicalresearchcoordinator #clinicaltrials #trials #drugdevelopment #drug #research #cra #crc #clinical
Link to the important videos:
Nuremberg Code: • Nuremberg Code and Naz...
Thalidomide Tragedy: • The Thalodomide Traged...
Tuskegee Syphilis Study: • Tuskegee Syphilis Stud...
Phases of Clinical trials: • What are Phase trials?...
Good Clinical Practices (ICH-GCP): • Good Clinical Practice...
Ethics Committee in Clinical Research: • Ethics committee in Cl...
NDCT Rules 2019: • New Drugs and Clinical...
SAE reporting and SUGAM: • Serious Adverse events...
Adverse events (AE) in Clinical Trials: • Adverse Events & Adver...
For queries/ contact please reach out at below mentioned platforms
Contact: 83900 88032 / 81778 96079
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docs.google.com/forms/d/135mI...
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In this video we talk about:
(0:00) Intro
(0:38) Protocol Fundamentals
(2:00) Protocol Details
(3:16) Trial background
(4:56) Study Design
(6:40) Participant Selection

[@goodthingsmotivation1776]

Sorry sir for unrelated comment
Sir i have got call from Bristol mayers for the position of vendor support specialist and current working as a CTA should I go for vendor support specialist. Is there a growth pls reply

[@clinicalresearchx360]

Thank you for reaching out. In my experience this profile has limited dimensions and would involve non-core job activities in regards to clinical trial conduct. I would suggest as per your current position go for a CRA role which would involve a lot of divorce activities to be done in proper core clinical trial conduct. Skip this profile if you can.

[@goodthingsmotivation1776]

@@clinicalresearchx360 thank you so much sirr