Services
Site Management Services (SMO)
Experienced study coordinators and site management associates who link investigators, sponsors and ethics committees, so your sites recruit on time and stay inspection-ready.
Request a proposal →ACRS supports Phase II–IV interventional and observational trials involving drugs, biologics, medical devices and surgical procedures.
Principal investigators get trained clinical research coordinators (CRCs) for daily trial activity and patient recruitment. Sponsors get site management associates for site oversight and ethics committee support.
Pre-initiation
- Identification of potential sites
- Fast feasibility
- Site set-up, supplies and infrastructure
- Regulatory and ethics committee communications
- Rapid clinical trial agreement (CTA) negotiation
- Site SOP set-up
During the study
- Dedicated, trained CRCs
- Patient recruitment and retention support
- Essential document maintenance
- Source documentation to ALCOA standards
- Investigational product accountability and storage
- CRF completion and query resolution within timelines
- AE and SAE reporting within timelines
- Support for monitoring visits, audits and inspections
Close-out
- Site close-out activities
- Destruction of used investigational product
- Archiving of site records
- Ethics committee notification of close-out and CSR
Discuss site management (smo) for your study
Tell us about your protocol, timelines and therapeutic area, and we will suggest how ACRS can support it.