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

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