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Blog

Beginner’s Guide to an Electronic Data Capture (EDC) System

An Electronic Data Capture system stores patient data collected in clinical trials. Learn the basics & functionality of EDC systems.

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4 min. read
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Blog

Deciphering the CRC Career Path: Key Skills and Responsibilities

Interested in becoming a clinical research coordinator? Understand the key skills and experiences sites look for.

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3 min. read
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Blog

Beginner’s Guide to Clinical Trial Performance Metrics

Learn what clinical trial performance metrics are, why they are important and which key metrics for clinical trials you should be measuring.

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4 min. read
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Secure Document Exchange

Accelerate study startup via end-to-end integration and automated, seamless exchange of research documents between sites, sponsors, and CROs.

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Oncology Clinical Research

Conduct fast & safe oncology clinical research with solutions that enable collaboration transparency and streamlined clinical operations.

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Research Evaluation System (EVAL)

Showcase Your Research ROI with EVAL. Demonstrate the impact of your research to the NCI, NIH and your organizational leadership.

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Participant Payments

Efficiently manage stipends and travel reimbursements across clinical trials with our automated payment system, integrated with OnCore CTMS.

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Research-Ready Training

Activate new sites and investigators efficiently with effective, engaging, and efficient training on introductory research and conduct essentials with our Research-Ready training.

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Electronic Source Data (eSource) + Electronic Data Capture (EDC) Platform

Streamline data collection, management, and compliance with Advarra's integrated electronic source data and electronic data capture platform.

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SiteIQ

Advarra's SiteIQ technology solution simplifies study startup and provides unparalleled visibility into site performance.

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Advarra Connect

A secure transfer of IRB-related documents directly from the CIRBI platform to your electronic trial master file.

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Advarra CIRBI Platform OLD

The CIRBI Platform enables real-time communication among sponsors/CROs, research sites, study staff and IRB members.

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