Clinical data is a key deliverable from a clinical research study. To this end, we have organized our Clinical Monitoring and
Data Management groups to work together as a specialized Data Collection Team. The team’s goal is to provide clean data for the
clinical database in a timely and efficient manner.
Clinical Expertise
- Broad therapeutic expertise
- Phase I through Phase IV trial management experience
- Networks of experienced investigators in the US and around
the globe
- CRA’s and Project Management staff are distributed throughout
the US and around the globe
Clinimetrics has core expertise in clinical research monitoring and we have assembled a strong team of CRA’s that are full-time
employees. Our CRA’s are widely distributed regionally throughout the US and around the globe, to provide our clients with
local expertise and responsive staff dedicated to their projects. They work closely with Data Management groups to form a
specialized Data Collection Team for each study.
Site Selection and Training
Clinimetrics maintains an extensive international database of investigators from which sites can be selected. We work with our
clients to identify sites for inclusion in studies. Our experienced CRA’s conduct pre-study site selection and qualification
visits at all identified sites. We ensure that all study sites are fully trained in the conduct of each research protocol. We
do this to assure the quality and integrity of the study on a prospective basis.
CRA’s Perform:
- Study site qualification
- Study initiation and site training visits
- Study site monitoring and close-out visits
- Source data verification
- Problem resolution
- Drug accountability reconciliation
- Regulatory document maintenance
- Site management activities to ensure successful study progress, including:
- Visit correspondence
- Telephone contacts
- Maintenance of study tracking logs
- Review of study materials
- Assistance with patient recruitment and retention techniques
- Query Resolution
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