Site Management (SMO)
End-to-End CRC Services with Proven Efficiency.and Quality
A Leading Site Management Organization (SMO)
Global MedTrial LLP is a trusted Site Management Organization (SMO) offering comprehensive, professional services to clinical trial investigators and research sites. We specialize in managing non-medical judgment aspects of clinical trials, ensuring enhanced study quality, streamlined processes, and greater standardization across all trial activities.
An optimal level of site management is critical to the success of clinical research. At Global MedTrial LLP, we support clinical trials from Phase I through Phase IV, with 70% of our projects sponsored by leading global pharmaceutical companies.
Site management is not just one of our services—it is the cornerstone of our mission. We go beyond basic site coordination and monitoring to deliver customized solutions that enhance site performance, ensure regulatory compliance, maintain protocol integrity, and protect patient rights and safety.
Skilled Clinical Research Coordinators
At Global MedTrial LLP, our Clinical Research Coordinators (CRCs) play a critical role in the successful execution of clinical trials. They are highly trained professionals committed to delivering exceptional quality, operational efficiency, and regulatory compliance throughout every phase of the research process.
High-Quality Execution
Ensuring accurate data collection, documentation, and reporting aligned with study protocols and regulatory requirements.
Timely & Cost-Effective Delivery
Adopting on-time and on-budget strategies while maintaining uncompromised quality.
Regulatory Excellence
Fully trained and compliant with ICH-GCP, GCP, and local regulatory standards.
Global Standards with Local Expertise
Upholding international benchmarks while offering personalized, site-level attention and strong customer service orientation.
Adaptability
Flexible to manage fluctuating workloads, protocol amendments, and evolving study timelines.
Looking to streamline your clinical research?
Partner with MedTrials Solutions for expert support in clinical trials from Phase I to IV, medical device studies, and non-interventional research. Our experienced CRC team is ready to assist you across multiple therapeutic areas.
Core Responsibilities
- Coordinating all aspects of clinical trial operations at the site level, including subject recruitment, screening, informed consent, and follow-up.
- Ensuring proper documentation, data entry, and query resolution in accordance with sponsor and regulatory requirements.
- Acting as the primary point of contact between the site, sponsor/CRO, and regulatory bodies.
- Supporting investigators with protocol adherence and regulatory submissions.
- Monitoring patient safety and reporting adverse events in compliance with study timelines.
- Maintaining accurate and complete trial records and essential documents.
- Contributing to audit readiness and continuous improvement initiatives.