Regional Study Coordinator
Covance inc
Total years of experience :3 years, 9 Months
I am responsible for the successful delivery of operations of a clinical study in their specific area of the world bridging the gap between the client and the site.
I monitor, track and provide resolution to all regional study queries and participate\ in functional meeting and provide input.
I communicate study milestones with my team and my client.
• I manage day-to-day local study related activities, especially logistics, monitoring and study supplies, keeping my team informed of any study development.
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Conduct eligibility screening interviews.
Assemble document and review reports for accuracy.
Ensure that all serious adverse events are reported on time and follow up with subject. Explain study procedures and obtain informed consent.
Communicate clinical trial status to management through meetings or others medical record data monitoring tools.
Create and update regulatory binder and schedule CRA’s monitoring visits.
Provide backup and support to all areas of clinical research.