SMO SERVICES

Alliance Site Network

ClinSite has an integrated network of specialised and top enrollers – clinical trial sites (CTS) across various regions in the world. Our network sites have established the necessary infrastructure, human resources, and facilities to conduct research within these centres. All the sites are GCP-trained sites and strictly follow Good clinical practices that ensure the integrity and quality of the data produced in the clinical trials at optimal study speed.

ClinSite’s, Alliance management team works closely with CRO’s and Sponsors desiring an efficient, well-coordinated network that consistently meets enrolment goals, builds high quality staffs, and maintains steady profitability.

Recruitment Support

ClinSite provide support to participants in accurately understanding the complete clinical trial and its process in its native language. Additionally, we oversee participant recruitment rate at clinical trial sites, and if needed, provide sites access to a broad network of referral recruitment through clinics, doctors, and satellite sites.

Site Management

ClinSite ensures that clinical trial sites adhere to relevant protocols and comply with GCP standards, leading to faster start-up times swift patient recruitment, precise documentation, and shorter study durations.
We leverage country-specific expertise to optimize efficiency in trial site selection, patient recruitment, and retention, ultimately saving time. Our network encompasses a range of sites, including general hospitals with various specialized departments such as gastroenterology, cardiology, infectious disease, neurology, endocrinology, and others.

ClinSite has contributed to the establishment and approval of GCP-compliant clinical trial sites having dedicated Clinical trial Units (CTUs). We aim to grow the pool of investigators and sites, leveraging the extensive experience of our alliance network sites across all therapeutic areas.

We offer a rapid and complimentary feasibility assessment for Sponsor/CRO requests through our extensive alliance network of clinical trial sites. Following Sponsor and protocol specifications, our expert team conducts a comprehensive 360-degree evaluation and identifies GCP-compliant sites for the project. A detailed site selection assessment report is then provided to the Sponsor.

Site Staff Training

ClinSite offers training sessions on protocols, study procedures, and local as well as international regulatory guidelines, ensuring compliance and authenticity in conducting clinical trials.

Clinical Trial Sites Reimbursement

ClinSite handles payments to the clinical trial sites and patient inconvenience allowance, thus, making it convenient for the Sponsor to check accurate invoicing against relevant activities and expense, calculating site fees, and processing payments in accordance with local tax requirements. This is achieved through the implementation of a service acceptance certificate, ensuring accuracy and compliance.