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Meghan Harrington

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Meghan Harrington
Meghan Harrington, MS
VP, Head of Site & Patient Payments

Meghan Harrington, MS, is Bioclinica's VP, Head of Site & Patient Payments and is responsible for the development and service delivery of all Bioclinica Site & Patient Payments SaaS technology products. Meghan and her team work with Sponsors and CROs to successfully outsource and implement Business Process Outsourcing (BPO) and Self-Service technology engagements.

Meghan has over 15 years of experience in the healthcare, technology and life science industries, which lends itself to a unique appreciation for both the needs and challenges of delivering top technology-enabled services in global clinical trials. Meghan is a subject matter expert in clinical trial payments and frequently presents at industry conferences and events.

 

 
 
 

 

Blogs

Site Payments Solutions

Site payments remain a challenge for sponsors – at Bioclinica, we have data to support this from our own Site & Patient Payments technology but also from surveys that we've conducted, most recently with FierceBiotech. A survey about site payments was distributed by FierceBiotech to sponsors in April 2018, and 149 sponsors responded.

Transformational Trends in Investigator Site Payments

At this year's DIA, I presented information about the pain points that the clinical trials industry is experiencing with regards to site payments as well as the trends that are currently occurring in this space – based on surveys, interviews and analysis of data in Bioclinica's Site & Patient Payments technology.

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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.

Bioclinica's #ClinicalDataManagement ecosystem of global experts, templates, coding tools and more fills the gap in… https://t.co/alXjYRaLd4
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With many clinical trials slowed or terminated, investments in new technologies are difficult. Yet, a #CTMS with a… https://t.co/VRIhWWf4tE
Bioclinica (3 weeks ago)
With Bioclinica #CTMS, sponsors & CROs have access to a full-featured, scalable system - a single, centralized sour… https://t.co/7ACrv8cvuF
Bioclinica (3 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 (4 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 (4 weeks ago)
Don't compromise with manual systems and spreadsheets. As an entry-level system with phased implementation, Bioclin… https://t.co/qIpi1MESXw
Bioclinica (5 weeks ago)