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Ann Marie Heiderich-LaDue

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Senior IRT Project Manager

Ann Marie has more than 10 years of experience as both a product manager and a project manager for IVR/IWR systems. In these roles she has been responsible for defining product features, meeting regulatory requirements, as well as directly managing system programming and deployments for dozens of international trials.

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With all of the decisions surrounding the launch of a clinical trial, choosing an IVR system to support your study can be a daunting task. Here are just a few of the things that you should look for when choosing an IVR/IWR system for your clinical trial organization.

  • Study build time
  • Ability to make last minute changes
  • Ability to support custom complex protocols

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Management Solutions

Bioclinica is organized into three business segments so that we can provide expert service and multifaceted technologies. Our Medical Imaging & Biomarkers segment includes an Imaging Core Lab, a Cardiovascular Safety division, and a Molecular Marker Laboratory. Our eHealth segment comprises eClinical Solutions, Randomization & Trial Supply Management, Safety & Regulatory Solutions, and Financial Lifecycle Solutions. Under the Global Clinical Research segment, we offer a network of research sites, patient recruitment, and a Post-Approval Research division.

RT @DrugInfoAssn: What has been the biggest takeway for your organization so far? Tweet @ us using #DIA2017
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"Q" on #RBM & Total Quality Mgmt? @Kristin_Mauri has "A" @DrugInfoAssn #DIA2017 https://t.co/MqCxkmAfa0
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Kristen Mauri shows the @DIA audience the value of risk based monitoring https://t.co/ssJCfc9gQ5
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Innovation Theater Kristin Mauri of @bioclinica presenting on RBM & TQM @DrugInfoAssn #DIA2017 https://t.co/zsGroQcpiU
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Innovation Theater @DrugInfoAssn #DIA2017 Kicking off at 1. Perspectives on risk-based monitoring and TQM. https://t.co/mH6Npg0kD4
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RT @Xtalks: How Improving Site Payments Can Make You the Sponsor/CRO of Choice Tune in for this live webinar with @bioclinica https://t.co/…
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