Clinical Data Management (CDM) | Interview Q&A | Clinical Data Management course #datamanagement #ai

Welcome to the world of Clinical Data Management, the backbone of successful clinical trials.
Are you preparing for an interview in this dynamic field? Or perhaps you’re just curious about what it takes to excel as a Data Management professional then this is the right video for you.
Today, we dive into data management as career filed and understand the data flow in clinical trials as well as learn about how to answer the most common interview questions and provide you with the answers that could land you the job
#datamanagement #data #interview #datascience #dataanalysis #career #dataquality #dataintegration #database #clinicalresearch #clinicalresearchassociate #blinding #masking #cra
#salary
Links Monitoring visit Series -
Blinding and Masking in Clinical Trials: kzbin.info/www/bejne/j57Pg6OnjM-Iq9k
ALCOA Plus Principles of Data Integrity: kzbin.info/www/bejne/nXLbo4Otd791i5I
Phases of Clinical Trials: kzbin.info/www/bejne/fpTWlKiujLSGea8
Links to most helpful videos:
CRA Interview: kzbin.info/www/bejne/qF6YgYGceq2KqKs
CRC interview: kzbin.info/www/bejne/sH6aaXhrd7OompY
Clinical Research Coordinator: kzbin.info/www/bejne/aIKxg3msbKitsLc
Clinical Research explained under 5 mins: kzbin.info/www/bejne/eYm2mWSQm5eNg6c
13 Principle of ICH-GCP: kzbin.info/www/bejne/inS6Zmihp7ytmJY
CRC or CRA: kzbin.info/www/bejne/qmrMh4KjZ7ycrK8
Phases of Clinical trials: kzbin.info/www/bejne/fpTWlKiujLSGea8
Good Clinical Practices (ICH-GCP): kzbin.info/www/bejne/q5jYnnWtrMeofdk
Ethics Committee in Clinical Research: kzbin.info/www/bejne/pKOynIWHn9l8pKs
NDCT Rules 2019: kzbin.info/www/bejne/fnfRamOeqrybo8U
SAE reporting and SUGAM: kzbin.info/www/bejne/epzGqIpngb2Xnck
Adverse events (AE) in Clinical Trials: kzbin.info/www/bejne/faTUhKFtlticmM0
For queries about Advanced Certification in Clinical Research, please reach out/contact at below mentioned platforms
Contact: [phone] / 83900 88032
To Register, please click on the link below:
docs.google.com/forms/d/135mI_tjvC-aojudmAPHUycpfLHGA64sdUMz2_XWRxUc
Instagram ID: clinical_aim_research
Gmail: [e-mail]
For any queries, kindly comment in the description box below.
In this video, We explain about:
(0:00) Intro
(1:18) What is Clinical Data Management?
(2:48) Data flow in Clinical trials
(5:15) Interview Q&A
(11:10) Position & Salary

[@abhradeepchatterjee8046]

Nice demonstration about scope and opportunities in CDM. THANK YOU SIR.

[@WealthWisdomHub99]

Your videos are excellent 👌🏻..im future u will have millions of subscribers for sure

[@share_market2k212]

Hello sir i have recently satrted as a fresher CRA in Monitoring BA BE studies and collect data, but my senior are saying that this experience of BA/BE studies is not useful as compared to CRA in Clinical trials monitoring , is that true ????? Please explain me as i am very confused

[@clinicalresearchx360]

Yes that is true to an extent. Because BA/BE trials are very niche and you won't be able to work on any other indications. BA/ BE trials are performed in a way and that's it, you won't get to learn more or update your skills. I agree with your senior, do not limit yourself to BA/BE. Try to work with others therapeutic trials and improve your portfolio. This way you would be relevant in the future as a CRA and not be restricted to a particular type of trials.

[@vinorengan]

Hii sir ,thank you for this videos. 2019 my passed out .year i m working as medical coder 4 yr experience .now i want to change CDM as a fresher it is possible sir ?

[@clinicalresearchx360]

Yes definately. Just make sure you study about the fundamentals of clinical research and clinical data management