Clincorp Technologies understands the importance of selecting a successful Clinical Trial Management Team, which includes, accounting for the complexity of a project, using effective management, and identifying the demands related to the execution of a project. Our team of Clinical professionals consists of highly experienced, trained, and dedicated Clinical Program Managers, Clinical Study Managers, and Clinical Research Associates committed to quality and compliance. Clincorp Technologies team brings a depth of experience in a broad range of therapeutic areas and a profound understanding of ICH, GCP, and FDA regulatory requirements to ensure the highest quality throughout all phases of development.

• Clinical Plan Development & Study Design
• Protocol Development
• CRO/Vendor Identification, Selection, and Management
• Investigator Selection
• Investigator and Subject Matter Expert Meeting Planning
• Study Activity Management
• Site Initiation, Management, and Close-Out
• Site Monitoring
• Key Opinion Leader and Study Investigator Communications
• Regulatory Strategy/Advisory Committee Input and Communications
• Regulatory Submissions