I am new to clinical trials and this has really helped me. Thank you!

Hey Dan... thanks for guiding..you are superb...your teachings are so very clear and helpful 👍🏻👍🏻

Thank you very much. Even as a drug development student I find this very useful!

I'm a finance guy and I understood a lot of it. I have been googling acronyms etc so I had some foundational knowledge. This is my second year in biotech.

I Love watching all of your videos!

@dansfera

7 жыл бұрын

DeeAnn Polacek thank you!

Excellent overview Dan

Thank you for all the great information!

@dansfera

6 жыл бұрын

+Lorrie Bisesi thanks Lorrie!

Thank you for this video, very useful content. Keep up this good work!

@dansfera

4 жыл бұрын

I appreciate you very much

Thanks!! Your videos are very useful!! Keep uploading please🙏🙏

@dansfera

6 жыл бұрын

thanks!

I have an interview for a clinical trial co-op so this is helpful!

Spot on. I've only just been working at IQVIA for about 1 year and I still feel like there are heappssss more to learn in the industry.

@ParagTechVideos

5 жыл бұрын

I am a recruiter for IMS Health for which position you are working on??

Dan, this is great content I like what I've seen I'm sure we could have some very advantageous conversations

@dansfera

6 жыл бұрын

Anytime reach out

love this video

@ramusunchu3211

6 жыл бұрын

Hii

Hello, this video is very good but, i also need to know about CRO in detail like all departments of CRO in detail.

Thank you for sharing.

@dansfera

2 жыл бұрын

Thanks for listening

Thank you so much! very informational! Do you have any video for tasks and activities from sponsor side as well?

@dansfera

Ай бұрын

Coming soon!

Awesome, indeed very useful, Thank you. :-)

Can you do a video explaining how to determine maximum tolerated dosage for Phase I trials?

@dansfera

6 жыл бұрын

I may need to interview a dr for that one, will do!

@spruceguitar

5 жыл бұрын

You need to be a PI or a sub-I for that competency. If you are an MD in a CRO for example you will get that training from the PI. But you really need solid experience at least as a sub-I in order to responsibly negociate that Protocol / ICF component with a Sponsor, and know when not to accept a very high dose of a molecule that Sponsors want to test in phase I or an IP that should not be administered without a concomitant (which Sponsors in phase I will push for btw, and the PI needs to know when to say no) etc. But if you want to learn that competency from a video that explains it I would strongly discourage you to do so. You can’t buy experience. Lots of responsibility, because the safety of the entire study hangs in that PI decision and whether he is able to successfully negociate the Protocol with the Sponsor.

Can you do a video on counting, maintaining, and destruction of the IP?

@dansfera

5 жыл бұрын

I will do one with Monica on this

thanks for this, you explain so simply yet professionally. what did you say about the medical liaison? the link between which two departments? thanks again

@ShivaDev2399

3 ай бұрын

Sales and R&D side of pharma

What EDC tools you use to collect data

Words come in real situations

Hi dan, how can I contact you directly via phone to discuss arranging a personalized consultation?

What does a clinical data manager do from start to finish of a clinical trial. What is the difference between the role played by a clinical data manager and a clinical trial manager in a CRO.

@dansfera

Жыл бұрын

Video soon

All were new at that time

have anybody been in such trials??? have you ever had any bad or permanent side effect??

Just got call from recruiter about Clinical QA manager position and they mention on the JD, that TMF experience required. I have 20 years experience in pharmaceuticals both commercial and clinical aspect, but primarily with deviations, CAPAs, SOPs, GMP training, and internal/external audits, a long with site wide metrics. Just trying to bridge my experience and see if my experience even relates somewhat with TMF. Is TMF completely different than what I mention in my experience? Just trying to prepare for upcoming interview Saturday. They seem real desperate to hire me and willing to pay high, but I dont want to set myself up for failure if i wont be able to do the work.... is it a Completely different animal? Any help greatly appreciated!!!

@dansfera

2 жыл бұрын

Where did you guys store records and documents

Does the site owner provide the subject for a study? Just want to understand. Thanks for you

@dansfera

Жыл бұрын

Yes they’re responsible for recruitment

Do you have a how to fill out or negotiate a CDA/NDA Agreement? What is considered standard language.

@dansfera

2 жыл бұрын

Will do

@patriciahaney3604

2 жыл бұрын

Thank you, Dan!

@patriciahaney3604

2 жыл бұрын

Thank you

Hi there, how to run a trial for my product? It's a wellness product. Thank you.

@dansfera

Жыл бұрын

Find regulatory consultant

Wisal elamin I need help becoming CRO

Hello Dan, Please share about artificial intelligence in clinical research And future

@dansfera

4 жыл бұрын

I have a few podcasts on that. Search my channel

I am new here. Please don’t use abbreviations. Thank you.

@dansfera

Ай бұрын

check the 4.5 hour video on my page and get the book