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Kevin Bishop

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Kevin Bishop
VP, RTSM

Kevin is a recognized clinical research senior executive with more than 30 years of operational and business leadership experience, the last 20 years of which have been in the high-growth eClinical technology space. In his current role, Kevin is responsible for driving the growth strategy for the Randomization & Trial Supply Management (RTSM) business, encompassing Bioclinica's innovative IRT platform, clinical supply forecasting, optimization and planning services, as well as further developing Bioclinica's unique project delivery methodology. Prior to Bioclinica Kevin led the RTSM and clinical logistics solution business at PAREXEL Informatics. Before that, Kevin was with ClinPhone for ten years focused on RTSM and other eClinical solutions before being acquisition by PAREXEL in 2008. Kevin has lived in the USA since 1999 when he relocated from the United Kingdom to facilitate the establishment of ClinPhone's business and North American operations. Prior to this he spent approximately ten years managing the execution of clinical development plans for various multinational pharmaceutical companies spanning all stages of pre-clinical and clinical research. Kevin has a Bachelor's degree in Physiology and Pharmacology from the University of Southampton (UK).

 

 
 
 
 

 

Blogs

Clinical Supply Chain Success: Leveraging Technology

The availability of investigational product often determines the success of a clinical trial's randomization and trial supply management (RTSM) solution. RTSM solutions are a key component of the clinical supply chain, the purpose of which is to ensure that the correct investigational product is at the right site at the right time for a subject.

Although we've largely moved beyond the initial implementation of clinical randomization and supply chain management systems (aka IRT) that were fully customized IT projects for each study to improved processes and more configurability, the industry now demands a more nimble, accurate solution, or "Agile" IRT.

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Leader in Clinical Trial
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.

With many clinical trials slowed or terminated, investments in new technologies are difficult. Yet, a #CTMS with a… https://t.co/VRIhWWf4tE
Bioclinica (2 weeks ago)
With Bioclinica #CTMS, sponsors & CROs have access to a full-featured, scalable system - a single, centralized sour… https://t.co/7ACrv8cvuF
Bioclinica (2 weeks ago)
Now available: a DIY #EDC solution. From study start-up to close-out, Bioclinica EDC Solo is an efficient, cost-eff… https://t.co/vFhC7ITfZV
Bioclinica (3 weeks ago)
Reduce the number of user requirement iterations and UAT findings during the #IRT build process. With the agile app… https://t.co/TJt2sZlrFP
Bioclinica (3 weeks ago)
Don't compromise with manual systems and spreadsheets. As an entry-level system with phased implementation, Bioclin… https://t.co/qIpi1MESXw
Bioclinica (4 weeks ago)
According to our recent poll, 45% of respondents had neither a #CTMS nor an #eTMF system, while only 24% had both.… https://t.co/l4dKC7pBQo
Bioclinica (4 weeks ago)