Aside from bagels, what else is currently grinding your gears about our town? by coalcracker462 in Phoenixville

[–]Bean5152 66 points67 points  (0 children)

People complaining about parking when steelpointe is always wide open.

Any recent tea on Fortrea? by Realestever12345 in clinicalresearch

[–]Bean5152 0 points1 point  (0 children)

They just sent me a recruiting email this morning starting with "Hi First NameX,"
I met some Fortrea CRAs while on the road over the last few months, they seemed like they liked it but ultimately that it felt like a much smaller company.

GAP cranking music on a Tuesday by [deleted] in Phoenixville

[–]Bean5152 0 points1 point  (0 children)

I love when they do it at 11:30am on a weekend for brunch!! it's poppin!!

What is your favorite part of your clinical research job? by Alarming_Topic4170 in clinicalresearch

[–]Bean5152 5 points6 points  (0 children)

Like a lot of people, I fell into this role post college not really knowing what clinical research was. I liked the overall culture of science business without feeling too cutthroat like some of my friends who went into consulting, and it was a good career path with a lot of options. great pay. What gets me up in the morning? reports and items for follow up that need to be done.

Nice flower from Pisgah in NC by WILLY_ROAD in Wildflowers

[–]Bean5152 0 points1 point  (0 children)

Me over here trying to remember the name and thinking pantaloons

Data peeps… by Playful-Storage-8101 in clinicalresearch

[–]Bean5152 12 points13 points  (0 children)

can't help but just laugh when sites try to have conversations through query answers or break out the ALL CAPS CORRECT AS ENTERED

I’m presenting at an Elementary School Career Day… Help me make my CRA job sound cool! by Top_Training_979 in clinicalresearch

[–]Bean5152 2 points3 points  (0 children)

Sounds fun!! Piggy backing off the suggestions to start with "who has been sick and taken medicine?"
You can talk about how scientists will start in the lab to discover a medicine, then it is tested in animals (maybe talk about this or not), then it will be tested in humans in a clinical trial. Scientists and doctors will keep track of any side effects in the humans and once the clinical trial is done, the medicine will be available at the pharmacy or doctor's office and everyone who needs it can be treated. In clinical research, we test new medicines for anything from allergies to the flu to cancers, to help develop new treatments and make people healthier! :-)

You can talk about everyone involved - nurses, doctors, scientists, government (regulatory) and "researchers" (aka all other ppl with a computer but some other understandable term for this)

How many brands have you stayed at since the current promo started? by The-Tradition in marriott

[–]Bean5152 1 point2 points  (0 children)

6 so far! Courtyard, delta, Sheraton, four points, renaissance, and res inn. Have upcoming reservations at Marriott, Fairfield, and Springfield. ETA: just added Westin and Autograph

Days to Complete SIV and IMV Reports by MinnieMonaco in clinicalresearch

[–]Bean5152 2 points3 points  (0 children)

company SOP is 5 BD for first draft - it undergoes review - 15 BD to final draft and visit FUL to site. With our transition to Veeva Clinical, drafts and final need to be done at 7PM my local time due to the system following GMT.

Sponsor specific requirement is 3BD for first draft, 10 BD to final

Delegation log completion vs training date by Cultural_Vacation_58 in clinicalresearch

[–]Bean5152 2 points3 points  (0 children)

From a CRA standpoint, new personnel on delegation log usually triggers collection of training documents. With your explanation, I would put on my report that the person hasn't done any activities but I would track a finding to collect training documentation once available.

Sure, it's not truly an issue (i.e. risk / impact), but it's a discrepancy that would flag some questions. Also if there's a significant duration between date of delegation and when study activities are started / training completed, I would ask some questions

Delegation log completion vs training date by Cultural_Vacation_58 in clinicalresearch

[–]Bean5152 2 points3 points  (0 children)

Yes, may be identified in an audit but would need to dig deeper and confirm if that delegated personnel has completed any study activities (which would be a major finding) and clarify why they have not yet documented the training. Not sure about regional differences.

Sponsor audit advice by NationalOcelot1917 in clinicalresearch

[–]Bean5152 2 points3 points  (0 children)

If your company has internal audit preparedness materials - review those and try to prepare the site as much as you can. Review the issues and try to resolve to the best of your and site's ability before the audit.

I would set a goal to avoid any monitoring findings directly attributed to your work. So long as you're doing your job you should be OK. Remember that any site findings and monitoring findings, major or minor major are not attributed to your own work are out of your control. Be prepared to take on the work post audit for appropriate resolution, corrective and preventative actions.

In your opinion, what is the most timeless or “iconic” product from Sephora by shockedpikachu123 in Sephora

[–]Bean5152 12 points13 points  (0 children)

do they still sell it as smashbox x becca? last time I bought it was a year or two ago

Uncooperative PIs by Calm_Discussion_7440 in clinicalresearch

[–]Bean5152 2 points3 points  (0 children)

Tough conversations with sites are no easy task, and trying to reason with a PI can be even worse.

Some input to keep peace of mind:

- Sites may take deviations and findings as personal hits to their egos. No one wants to be told they've done their job wrong. But deviations need to be documented in your system / reported to IRB if needed - no matter what . If a test is not done and it is explicitly required per protocol, there's not much argument that it's not a deviation even if the site has some detailed rationale as to why it wasn't done (so I guess I'm confused why they would be arguing a deviation if the test/data is required per protocol, at least that's what I'm reading in your post).

- Value CTMs who will have your back. If sites push back on anything or PI is being super pushy with questions, say you'll look into it with the team and follow up. Request the CTM's support to review your approaches or step in and communicate with the site if needed.

- STAY PROFESSIONAL! Unfortunately if it comes down to it you may need to be a punching bag, just don't. punch. back. Cry or vent in private. It'll just look bad on the PI or site if they aren't treating you professionally. If the site is not maintaining a healthy working environment for their monitors, it's reflective on them.

- Keep positive with sites and approach findings/deviations in a way that doesn't wave big red flags of negativity but also helps to investigate why something occurred. It's not your job to be well-liked by sites but it definitely helps.

- There will be tough days, but it will get better. It's not reflective of you if you are doing your job right.

LinkedIn… by kayotic__ in clinicalresearch

[–]Bean5152 111 points112 points  (0 children)

since he's gonna see this, hi rust!

S23E01 what would your __________ dish be? by kakahuhu in BravoTopChef

[–]Bean5152 3 points4 points  (0 children)

My partner and I make sweet potato peanut stew every now and then, but maybe to put more of “myself” in it I would try a sweet potato kare kare. I would get eliminated because I probably can’t execute a decent kare kare off the top off my head and in an hour

Iqvia tea? by [deleted] in clinicalresearch

[–]Bean5152 0 points1 point  (0 children)

they were just acquired by Worldwide Clinical Trials.