Clinical Research Services

At Concentrics, our staff has conducted over 600 clinical trials in various therapeutic areas during the last 21 years. We offer a wide range of CRO services in the area of clinical research.

•    Phase II
•    Phase III
•    Phase IIIb
•    Phase IV

Our Clinical Division has created an environment that attracts and retains talented employees. Our research staff members have multiple years of research experience, participate in regular training including ICH/GCP guidelines, and several staff members are CCRC certified. Many staff members have worked in clinical site management early in their careers, allowing them to relate and understand the needs of the sites.

As a value-added service to our clients, our internal Quality Assurance Department routinely audits our work to ensure quality excellence in the trial.

We offer the following suite of services to our clients:

Design Team   •Research Design Consultation   •Protocol Development Project Management   •CRF Development   •Key Study Document and Tools Development   •IRB Submission   •Site Selection and Contracting   •Site Management   •Patient Recruitment   •Safety Surveillance   •Monitoring Data Management   •Double Data Entry and Reconciliation   •Edit and Logic Checks, Query Resolution, Adverse     Event and Concomitant Medications Coding   •Data Analysis and Biostatistics   •Medical Writing   •Report Writing