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Barbara Clendenen

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Barbara Clendenen, MBA
Barbara Clendenen, MBA
Director, Business Development, Drug Safety and Regulatory

Barbara Clendenen, MBA, designs Pharmacovigilance and Regulatory solutions that increase compliance and reduce risk for life science organizations. She has over 20 years of experience blending both science and business expertise to assist pharmaceutical, biotech, medical device, and CRO clients in meeting research and post marketing goals. She began her career as a research scientist in Immunology and Oncology.  Since 1998, she has held pivotal roles in business development and sales management within the scientific and clinical research industry for Becton Dickinson, Fisher Scientific, and Bio-Rad. Prior to joining Bioclinica in 2015, she led the Business Development Team at Quorum Review IRB, developed the organization's entry into the hospital and AMC market, and participated in CIRB (Consortium of Independent Review Boards). Barbara graduated from University of Washington with a Bachelor's degree in Microbiology and from Seattle University with a Master's in Business Administration.

Blogs

The electronic common technical document (eCTD) is an interface for the pharmaceutical industry to transfer regulatory information based on the Common Technical Document (CTD) format, which is an agreed common format for applications that will be acceptable in all three ICH-Regions (US, EU & Japan) and other countries.

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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.

Congrats @bioclinica on @Clin_Info_News Best Practices Award 4 "Transformational Med. Imaging in #ClinicalTrials. '… https://t.co/NxauNywq23
bioclinica (Yesterday)
RT @BrianSMcGowan: Allison Proffitt Editor of Clinical Informatics News, Best Practice Awards @ from Clin_Info_News ... recognizing applied…
bioclinica (3 days ago)
@Clin_Info_News @IQVIA_global @CRFHealth All of us @Bioclinica are truly honored to receive this recognition. Congr… https://t.co/mULb8tatJ2
bioclinica (3 days ago)
RT @Clin_Info_News: Congrats again to @IQVIA_global @CRFHealth @bioclinica on winning the @Clin_Info_News Best Practices awards at #SCOPE20…
bioclinica (3 days ago)
And the winner is! Transformational Medical Imaging in #ClinicalTrials: @bioclinica SMART. @Clin_Info_News Best Pra… https://t.co/IYZoWoK8CB
bioclinica (3 days ago)
Folks at #SCOPE2018 hearing from Eric Forsthoffer and Rebecca Lupo about Bioclinica's Site Network.… https://t.co/aHRJtHb6zz
bioclinica (3 days 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