Study
Feasibility
Our initial study feasibility can provide some forecasting related to estimation of patients, sites, and estimated time required to deliver the study from start to finish. Help our sponsors identify issues related to recruitment projection, as well as review the competitive regional landscape
Study Start up
Activity
Our proficient team members will ensure that all the ts are crossed and is are dotted, while submitting deliverables in a timely manner in the following areas:
- Study and Development of Protocol
- ICF & CRF/eCRF development
- Clinical Development Plans (PM, Monitoring, Quality, Communication, etc.)
- Final Investigator/site selection & patient recruitment strategies
- Preparation and conduction of Kick off meeting.
- Investigator Meeting Planning and execution
Project
Management
We place great emphasis on providing both quality services and project management to our sponsors. Our goal of providing outstanding services, technical leadership, and scientific expertise is achieved at an operational level by employing a matrix based organization model for its management structure. Under this matrix, we assign a dedicated team of professionals to each study. The project team is formed across functional groups, with individuals assigned based on their levels of experience. This matrix is well suited to the interdependency between stakeholders, and allows for an integrated, multi-disciplinary execution of project objectives. Additionally, we utilize a comprehensive suite of project management tools, and processes to streamline overall study management, reporting, and risk mitigation.
Site
Management
Active communication: In order to ensure that the trial is a success for all parties, our team will ensure that Continuous Regulatory documentation updates and maintenance are in accordance with Regulatory Agency’s Guidelines. Our processes include active communication with the Investigator, Site, Sponsor and Vendor from startup until publication.
Real world evidence
& Late phase
CCORN offers core capabilities to help our clients to achieve their commercial and scientific objectives, with a highly qualified team who leads our RWE (Real World Evidence) and late phase research efforts in the Hematology and Oncology space.
Our team touts over 100 years of collective experience in Clinical and Observational research, and many publications in areas including.
Hematology, Oncology and practice transformation. We offer wide array of research services including RWE (Real World Evidence), Registries, Health Economics and Outcomes Research.
Therapeutic
Areas
With decades of our expert team’s combined Clinical and Research experience our focus area is serving our clients in the Hematology/Oncology space. As an emerging company, with an innovative approach to RWE and Registry studies, we are confident in serving our clients with dedication and an innovative approach.
Community Clinic
Integration
“CCORN uses a network of community clinics to distribute trials to appropriate locations. Our sites create a profile of physicians with experience ranging from Phase 1 to Registry studies, as well as a patient demographic that more completely represents that of the cancer patient population. By enrolling a broader range of patient profiles, CCORN decreases the disparity in clinical trial representation and ultimately contributes to the optimization of Precision Medicine.”