Services

Project Management

C3 can manage a study and vendors from start to finish or work in conjunction with in-house management. C3 customizes management tools for each project to track and analyze (enrollment, study supplies, visits & reports, etc.) Our keys to successful project management is developing reasonable expectations with clear communication.

On-site and Remote Clinical Monitoring

C3 can conduct Pre-Study, Initiation, Interim/Routine and Close-Out visits for all phases of clinical trials on-site or remotely. Our senior Clinical Research Associates can effectively manage sites as well as meet and exceed data milestones.

Data Review and Management

C3 has data management consultants that can design CRFs for paper or eDC studies. Our data management consultants can work with data management vendors to ensure appropriate queries and manage data cut timelines in order to meet study milestones.

Regulatory, QC, and GCP Audits

C3’s clinical professionals can perform on-site regulatory, QC and GCP audits. Our clinical professionals can also work with sites or companies to develop and/or streamline processes following an audit.

Document Management

C3 can collect, compile, track and review for compliance documents essential in study start-up. C3’s key to smooth start-up is to stagger the focus of each deliverable in a systematic approach to streamline the entire process.

Electronic Trial Master File

C3 uses a secure online document storage platform which allows users to access the electronic Trial Master File 24/7. Please visit e-Trial Master File for more information.

Feasibility Studies, Recruitment

C3 can generate, disseminate, collect, and compile customized feasibility questionnaires for any upcoming clinical trial. C3 will analyze the compiled information into a comprehensive report. C3 will provide recommendations and risk mitigation strategies based on the recruitment goals and study timelines.