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Kevin Bishop

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Kevin Bishop
Global Vice President & General Manager Randomization & Trial Supply Management

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, and optimization clinical supply forecasting and planning services, as well as further developing Bioclinica's unique project delivery methodology. Most recently Kevin led the RTSM and clinical logistics solution business at PAREXEL Informatics. Prior to this, Kevin was with ClinPhone for ten years focused on RTSM and other eClinical solutions prior to 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).

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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.

RT @SchulmanIRB: #FDA final rule requires #medicaldevice #research conducted outside US to conform with GCP standards | via @RAPSorg https:…
bioclinica (14 hours ago)
RT @manchempharma: Paul Brooks, Executive Director, @RAPSorg comments on Brexit and the operational trade and regulatory environment affect…
bioclinica (14 hours ago)
RT @eClinical_Jen: Clinical Data Management articles available on SCDM Website - While all articles are available to members, there are sel…
bioclinica (14 hours ago)
Live from Las Vegas where Bioclinica's Research Development Director Marieke Cajal, PhD, is presenting on site star… https://t.co/lVglg6NWdV
bioclinica (15 hours ago)
Many thanks all who attended @bioclinica's Executive Roundtable on Safety Mgmt for Pharma Cos in Japan in Tokyo th… https://t.co/OzHeSvHTUk
bioclinica (15 hours ago)
RT @bioclinica: @CardiacSafety Consortium needs your feedback! Help make the upcoming think tank "Evaluation of #MobileTechnologies in #CV…
bioclinica (17 hours 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