Our experienced site management team is dedicated to ensuring the efficient, ethical, and compliant conduct of clinical trials. We collaborate closely with sponsors, CROs, and investigators to support every phase of the research process—from study startup to close-out.
Our Site Management Services Include:
1. Study Startup Support
- Site feasibility and selection assistance
- Regulatory document preparation and submission
- IRB/EC coordination and communication
- Site initiation and staff training
2. Clinical Operations Oversight
- Coordination of day-to-day trial activities
- Investigator and site staff support
- Monitoring visit preparation and follow-up
- Patient recruitment and retention strategies
- Protocol compliance monitoring
3. Regulatory Compliance & Quality Assurance
- Adherence to GCP, ICH, FDA, and other regulatory standards
- Ongoing internal audits and quality checks
- Timely safety reporting and deviation documentation
4. Data Management Support
- EDC training and data entry oversight
- Query resolution and source document verification
- Collaboration with CRAs and data managers
5. Site Close-Out and Archiving
- Final data reconciliation and query resolution
- Essential document archiving
- Site close-out visit support
Why Choose Our Site Management Team?
- Dedicated, experienced clinical research professionals
- Proven track record of successful site operations
- Robust SOPs and QA processes
- Commitment to participant safety and data integrity