Clinical Research Monitoring and Site Management

ClinWin staff on site.

ClinWin retains a team of experienced Clinical Research Associates (CRA's) to monitor and manage clinical trials. Initiation, monitoring and close out visits are run according to sponsors' requirements and reporting methods, documented in the Clinical Monitoring Plan. Our experience ranges from Phase I-IV trials across a range of organisations and therapeutic areas.
Our staff are trained on Good Clinical Practice (ICH-GCP), Good documentation Practices, Standard Operating Procedures (SOP's), Electronic Data Capture, Clinical Trials Management Systems (CTMS), scientific and medical topics, and updates on industry developments.
Our CRA's work closely with the sites, and we have developed cordial relationships with site staff. All studies have a lead and a back-up CRA.

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