Clinical

Trial Management and Clinical Operations

At Alira Health, our mission is to deliver effective, end-to-end resource planning, collaboration, and training for our clinical trial partners.

We offer a holistic, well-coordinated, and collaborative approach that leverages our in-depth experience with site, investigator and vendor relationships, creating successful trials that satisfy fast start-up timelines and complicated regulatory environments.

Additional clinical operations services

Your Alira Health team can also provide support services including:
  • Collection, review, and approval of essential site documents
  • IRB/EC submission assistance
  • Set up and maintenance of the TMF
  • Monitoring of site source data against the CRF/eCRF
  • Monitoring of site regulatory documents
  • Quality Assurance (QA) audits of clinical trial sites

Why choose Alira Health?

With Alira Health industry leading CRO as your partner, you will benefit from:

  • Exceptional customer service and site relations
  • In-depth expertise across the entire clinical trial process
  • Flexible and tailored service delivered by multidisciplinary and global teams
  • Frequent, transparent, and professional communication
  • Guarantee we will lead your study efficiently, safely, and successfully

Related News

Clinical
News June 8, 2021
Alira Health Expands Its Global Clinical and Data Capabilities Through the Acquisition of CROS NT
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News January 7, 2021
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Publications September 4, 2020
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