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Kenneth Clark

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Kenneth Clark
Vice President, RTSM Professional Services

Ken Clark has been involved with IRT systems since 2003, back when they were still called IVR systems, and occasionally "IWR." He has seen the RTSM industry from many angles. He led the development team which created one of the industry's first parameterized IRT systems for a top 5 pharma client in his early years. After that, he managed the development and multi-partner integration programs for a global clinical inventory management and QA system, also for a top 5 pharma client. Since then, he has served as the head of the Bioclinica Consulting Group and most recently as Bioclinica's Vice President of RTSM Professional Services, covering delivery of all RTSM services, encompassing RTSM project management, RTSM consulting services, RTSM operations, and clinical supply chain optimization. He is currently Vice President of RTSM Product Delivery, responsible for Bioclinica's suite of RTSM applications, including the Trident IRT.

Blogs

The clinical randomization and supply chain management systems we now dub “IRT” were initially built as fully customized IT projects, individualized and implemented separately for each study. While the processes have improved since then and some IRT providers are now using systems designed for more configurability, the mindset of customizing IRT systems for each study persists.

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Management Solutions

Successful clinical trials require the ability to see key details and uncover hidden insights. Bioclinica utilizes science and technology to bring clarity to clinical trials, helping companies to develop new life-improving therapies more efficiently and safely.

If study sites R asking 4 accuracy & speed in site payments & the clinical financial folks R demanding better budge… https://t.co/FR4QE2QEqx
bioclinica (1 hour ago)
See you at #DIA2018 ! Here's when & where to find @Bioclinica in our exhibit, at Innovation Theater (Site Payments!… https://t.co/z4hPha2Ppo
bioclinica (Yesterday)
Reminder: Today's webinar on Clinical Endpoint Adjudication kicks off at 1 PM Eastern. > https://t.co/1IU9TVFCFA
bioclinica (5 days ago)
In a new go-to-guide on conducting #Alzheimer's clinical trials, @bioclinica experts Joyce Suhy, Marieke Cajal, Luc… https://t.co/SaBFm3L9CL
bioclinica (5 days ago)
Clinical Endpoint Adjudication Webinar. Join us in a live online event this Friday, (6/15) Details & reg. > https://t.co/uBjlgSMnDS
bioclinica (6 days ago)
Clinical Endpoint Adjudication webinar this Friday! Interested in establishing a universal clinical vocabulary to i… https://t.co/uPD992tSaY
bioclinica (1 week ago)

Latest Blogs:

Latin America: Benefit from the Right Partner
Removing Risk from Clinical Trial Management System (CTMS) Implementations
Collaboration Between Clinical Operations and the Logistics and Supply Chain Teams is Key to Trial Success
The Value of Protocol Review
CTMS and RBM: Hot Topics at OCT Nordics in Copenhagen