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.
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