Clinical
Trial Management and Clinical Operations
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.
Comprehensive operations support
The dedicated Alira Health team acts as an extension of our sponsor’s teams and provides seamless support at every stage of the development process—from study feasibility and site selection to study close-out.
Our support services include:
Timeline Creation and Analysis
Site Feasibility and Qualification
Site and Investigator Selection
Site Management
Site Monitoring
Additional clinical operations services
- 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