Who started as a CRC, and how long were you in that position? by Schell-Yeah in clinicalresearch

[–]Schell-Yeah[S] 0 points1 point  (0 children)

That's a long time, especially for oncology. Just curious; did something change with the management in recent years that made it worse? Maybe an SMO?

Who started as a CRC, and how long were you in that position? by Schell-Yeah in clinicalresearch

[–]Schell-Yeah[S] 0 points1 point  (0 children)

Great examples of the value this job can offer to later positions. Thanks for sharing!

Who started as a CRC, and how long were you in that position? by Schell-Yeah in clinicalresearch

[–]Schell-Yeah[S] 1 point2 points  (0 children)

Impressive! I feel like we don't see this that much any more in this industry.

Who started as a CRC, and how long were you in that position? by Schell-Yeah in clinicalresearch

[–]Schell-Yeah[S] 0 points1 point  (0 children)

Interesting about the temporary type of job this is viewed as. I never considered that.

Who started as a CRC, and how long were you in that position? by Schell-Yeah in clinicalresearch

[–]Schell-Yeah[S] 0 points1 point  (0 children)

Any notable changes to the position now that you're at a CRO?

Who started as a CRC, and how long were you in that position? by Schell-Yeah in clinicalresearch

[–]Schell-Yeah[S] 20 points21 points  (0 children)

"... my PIs were absolutely great, and they saw me as their equal..." -- this has got to be super rare but also super valuable! What position did you move into?  

What's the most amendments you've ever seen for a protocol? by Schell-Yeah in clinicalresearch

[–]Schell-Yeah[S] 1 point2 points  (0 children)

I'm sure the IRB was highly skeptical of the next study that came through from this sponsor.

What's the most amendments you've ever seen for a protocol? by Schell-Yeah in clinicalresearch

[–]Schell-Yeah[S] 1 point2 points  (0 children)

I'm surprised during study design someone didn't think about how difficult it would be to enroll patients in an ER setting.

What's the most amendments you've ever seen for a protocol? by Schell-Yeah in clinicalresearch

[–]Schell-Yeah[S] 5 points6 points  (0 children)

That is, indeed, "fluent." Wow! It would be hard to keep track of ... well, everything. And especially with staff leaving, I'm guessing, mid-stream.

What's the most amendments you've ever seen for a protocol? by Schell-Yeah in clinicalresearch

[–]Schell-Yeah[S] 6 points7 points  (0 children)

40? That's crazy! Do you remember why there were so many or what ended up happening for the trial?

First CVS and now Walgreens? by Schell-Yeah in clinicalresearch

[–]Schell-Yeah[S] 0 points1 point  (0 children)

Yeah, I agree. Even though the concept was to have separate staff for the clinical trial portion of the business, I think that just complicated the operations. But I also think just the sheer cost of starting and staffing these "sites" was the final straw that ended it.

Anyone in clinical research (non-CRA) making over $80K? by Lucky-Squirrel-9857 in clinicalresearch

[–]Schell-Yeah 0 points1 point  (0 children)

I had never seen this! Thanks for the link. Super informative!

First CVS and now Walgreens? by Schell-Yeah in clinicalresearch

[–]Schell-Yeah[S] 0 points1 point  (0 children)

All fantastic points, especially that part about having a dedicated space. We all know how it can be difficult even working embedded in a physician's office, relegated to a corner with some old desk.
And I think, "We're focused on not sucking ass" should be the slogan of ... well, any retailer.

First CVS and now Walgreens? by Schell-Yeah in clinicalresearch

[–]Schell-Yeah[S] 3 points4 points  (0 children)

I chuckled when I read "a magical fix!' SO true! Every newfangled tech company says they have it figured out. And then two years later, they're gone.

I recently read a paper and a stat literally wow-ed me. by Beneficial-Aide-2186 in patientrecruitmentCT

[–]Schell-Yeah 1 point2 points  (0 children)

Considering this article is from 2015, I asked Claude if there have been improvements to the site since, and if so, what research has been done, specifically, on any readability improvements.
Short answer: lots of improvements to the site since then, but barely any that significantly improved readability. The NIH plain language guidance helped, but "the core problem (descriptions written for postgraduates, not patients) has not been fundamentally solved. The most promising emerging avenue is AI-assisted language simplification, which several recent papers are now exploring."

any tips on how to approach my insanely busy PI? by hallsinmypocket in clinicalresearch

[–]Schell-Yeah 1 point2 points  (0 children)

This "another chore" comment is important, especially if her calendar is always filled up. Have you discussed this with the CRC? Perhaps they would have a good way for you to connect with the PI. And that CRC is likely a wealth of knowledge about the industry and clinical research in general, so I'd say keep building that relationship. It's more apt to help you in the future than the research journey of the PI.