
Clinical Trial Coordinator
Support clinical study team(s) as a specialist in document management Collect, review and file clinical trial documents; identify and track issues to resolution. Prepare, manage and archive clinical trial documentation in accordance with applicable regulations. Conduct quality checks of clinical trial documentation/files. Prepare shipments, maintain stock levels and lead tracking and reconciliation of study supplies. Assist with accruals, site and vendor payments, and maintenance of payment systems. Build and maintain study-specific tools (e.g., site lists, contact information). Handle the generation, translation, assembly and distribution of study materials. Support trial sites directly/indirectly through assigned site managers, as needed. Generate and disseminate trial correspondence including newsletters, global correspondence, etc. Handle confidential and proprietary information in accordance with applicable laws and regulations.
At least 2-3 years supporting clinical trials in an administrative capacity
Working knowledge of Good Clinical Practice and FDA regulations
Ability to work on multiple projects simultaneously
Documentation
Time Management
Analytical skills
MS Excel
MS Word
Verbal communication
Detail Oriented
written communication
Multitasking Skills
Adaptability
According to JobzMall, the average salary range for a Clinical Trial Coordinator in Building 1, 1000 Lake Hazeltine Dr, Chaska, MN 55318, USA is $60,000 to $70,000. This salary range is based on the geographic location, experience, and skill set of the individual.
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Beckman Coulter Inc., is a Danaher Corporation company that develops, manufactures and markets products that simplify, automate and innovate complex biomedical testing.

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