Site & Patient Management
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Site & Patient Management
Site & Patient Management: Enhancing Clinical Trials Across 50 Cities
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CSC's Comprehensive Approach
With over 350 strategically positioned Clinical Research Coordinators (CRC) spanning 50 cities, CSC ensures immediate and widespread coverage whenever and wherever needed. Our Site Management Organization (SMO) plays a pivotal role in optimizing investigator engagement and alleviating the burdens faced by investigational sites, especially in densely populated areas lacking specialized care. -
Site Management Organization (SMO): Challenges in China
In China, the unique challenges arise from the dense population and insufficient specialized care in rural regions. This results in a heavy workload for many investigational sites and esteemed investigators, extending beyond their designated responsibilities. The burden impacts study performance and diminishes investigators' enthusiasm for participating in complete clinical trials over time.
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CSC Clinical Research
Our CRC are dispatched to investigational sites served as investigators’ assistant, handling administrative tasks throughout the clinical trial process. Tasks include identifying potential patients, updating eCRF(electronic case report forms) managing subjects, filing documents, and facilitating interdepartmental communication. While most CRC members are certified nurses with ample medical knowledge to assist investigators, they do not participate in medical determination procedures. With CRC support, investigators can dedicate themselves to their primary focus—Subjects’ Treatment.
Sponsor & CRO
Feasibility Study
Investigational sites recommendation
EC Submission Support
Experimental Contract Signing Support
Subjects Follow-up Support
CRF & EDC Upload
Subjects Recruitment
Multidisciplinary Communication and Writing
CSR Collection
Investigational Sites Close Support
Project Management
Clinical Study Management
Qualified and Experienced CRC Support
Recruitment Planning
Data Management
Independent Protocol Audit
Site Management
SOP Implementation and Accreditation of Investigational Sites
Audit
NMPA Inspection Support
Education Training
Trainings for Investigators & Others personnel
Site Business Development and Promotion
Introducing more projects and promoting business capabilities
Seeking potential cooperation business opportunities
CSC's holistic approach to site and patient management ensures seamless and efficient clinical trials, enabling investigators to focus on what matters most—providing optimal treatment to subjects.