Clinical Research Consultants, LLC.

Clinical Research Consultants, LLC. Offering 15 years of Clinical Research and Regulatory Development experience for pre/post IPO.

11/29/2023

🟠 Are you a PI looking for some assistance in conducting protocol-specific Study Visits (on-site and off-site) for your site’s clinical trial(s)?

🟠 Has your site/Sponsor struggled to enroll volunteers per local COVID-19 restrictions and need home-based study visits from qualified Research Professionals?

🟠 Is your site’s turn-over rate for employees so high that you are unable to depend on workers and meet regulatory deadlines?

🌺 Let us help you… We have over 17 years of experience in clinical trials, from start-up to close-out, from regulatory guidances to clinical operations, and everything that makes for a successful study completion. 🌺

🐳 We can also go directly to the Subjects home to conduct each study visit per the protocol’s “Schedule of Activities” so Volunteers do not need to leave their houses at all, if they so choose. We also offer general Regulatory and Clinical Development oversight, consulting and training, including site monitoring. 🐳

🐠 Services include but are not limited to: physical exams, EKG, vitals, data entry into EDC, EDC/source document creation, specimen collections & processing, recruiting and assistance with study-related activities such as a source of support between the PI & Study Volunteers. 🐠

☀️ JUST ASK, WE WILL ACCOMMODATE ☀️

Even with love in the air, we have to work hard!❤️ Are you a PI looking for some assistance in conducting protocol-speci...
02/17/2023

Even with love in the air, we have to work hard!

❤️ Are you a PI looking for some assistance in conducting protocol-specific Study Visits (on-site and off-site) for your site’s clinical trial(s)?

❤️ Has your site/Sponsor struggled to enroll volunteers per local COVID-19 restrictions and need home-based study visits from qualified Research Professionals?

❤️ Is your site’s turn-over rate for employees so high that you are unable to depend on workers and meet regulatory deadlines?

💕 Let us help you… We have over 17 years of experience in clinical trials, from start-up to close-out, from regulatory guidances to clinical operations, and everything that makes for a successful study completion. 💕

🕊️ We can also go directly to the Subjects home to conduct each study visit per the protocol’s “Schedule of Activities” so Volunteers do not need to leave their houses at all, if they so choose. We also offer general Regulatory and Clinical Development oversight, consulting and training, including site monitoring. 🕊️

❤️ Services include but are not limited to: physical exams, EKG, vitals, data entry into EDC, EDC/source document creation, specimen collections & processing, recruiting and assistance with study-related activities such as a source of support between the PI & Study Volunteers. ❤️

🥰 JUST ASK, WE WILL ACCOMMODATE 🥰

❄️ Are you a PI looking for some assistance in conducting protocol-specific Study Visits (on-site and off-site) for your...
01/23/2023

❄️ Are you a PI looking for some assistance in conducting protocol-specific Study Visits (on-site and off-site) for your site’s clinical trial(s)?

❄️ Has your site/Sponsor struggled to enroll volunteers per local COVID-19 restrictions and need home-based study visits from qualified Research Professionals?

❄️ Is your site’s turn-over rate for employees so high that you are unable to depend on workers and meet regulatory deadlines?

⛄️ Let us help you… We have over 17 years of experience in clinical trials, from start-up to close-out, from regulatory guidances to clinical operations, and everything that makes for a successful study completion. 🌺

❄️ We can also go directly to the Subjects home to conduct each study visit per the protocol’s “Schedule of Activities” so Volunteers do not need to leave their houses at all, if they so choose. We also offer general Regulatory and Clinical Development oversight, consulting and training, including site monitoring. 🐳

⛄️ Services include but are not limited to: physical exams, EKG, vitals, data entry into EDC, EDC/source document creation, specimen collections & processing, recruiting and assistance with study-related activities such as a source of support between the PI & Study Volunteers. ⛄️

❄️ JUST ASK, WE WILL ACCOMMODATE ❄️

01/17/2023
10/10/2022

Wishing everyone a safe & happy Autumn 🍂

Specialists in conducting clinical trials using good clinical & documentation practices (GCP and GDP) under the auspices...
09/22/2022

Specialists in conducting clinical trials using good clinical & documentation practices (GCP and GDP) under the auspices of a Sponsor/Principal Investigator (PI). Contact us today to get your research project off the ground, from start-up to close-out! 🧬 🩸 🦠 💊

06/01/2021

Let us help manage all of your clinical trial needs, from start-up to close-out... and everything in between!

NEW YEAR CALLS FOR A NEW WAY TO CONDUCT TRIALS!🔵 Are you a PI looking for some assistance in conducting protocol-specifi...
01/04/2021

NEW YEAR CALLS FOR A NEW WAY TO CONDUCT TRIALS!

🔵 Are you a PI looking for some assistance in conducting protocol-specific Study Visits for your site’s clinical trial(s)?

🔵 Is your site facing shut-down orders per local COVID-19 restrictions because COVID is still on the rise?

🔵 Are your research staff unable to come into work because they are at home in self-quarantine?

🤓 Let us help you! We have over 15 years of experience in clinical trials from start-up to close-out, from regulatory guidances to clinical operations, and everything in between that makes for a successful study!

💪We go directly to the Subjects home to conduct each study visit per the protocol’s “Schedule of Activities” so Volunteers do not need to leave their houses at all. In most cases, we perform the visit outside or even in their garage, all to adhere to social distancing and COVID-19 guidelines recommended by the CDC.

💚 Services include but are not limited to: physical exams, EKG, vitals, data entry into EDC, EDC/source document creation, specimen collections & processing, recruiting and assistance with study-related activities such as a source of support between the PI & Study Volunteers. 💚

Specialists in conducting clinical trials using good clinical practice (GCP) under the auspices of a Principal Investiga...
07/08/2020

Specialists in conducting clinical trials using good clinical practice (GCP) under the auspices of a Principal Investigator (PI). Contact us today to get your research project off the ground! 🧬 🩸 🦠 💊

Address

Cheshire, CT
06410

Telephone

+12038268831

Website

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