
Clinical Study Coordinator
Há 11 horas
The Clinical Study Coordinator will be responsible for the setup, organization, and maintenance of clinical study documentation. This includes preparation for internal/external audits, final reconciliation, and archival.
This role requires an ability to travel as needed, with at least 60% of the time dedicated to this activity. The coordinator must also have a willingness to acquire knowledge of ICH GCP, clinical trials, and governing regulations.
Required Skills and Qualifications- Bachelor's degree in life sciences or a related field
- Associate degree in nursing
This is a developmental role that offers extensive training and opportunities for growth.
OthersThe Clinical Study Coordinator will work closely with project teams to ensure study files are inspection-ready at all times. They will also assist with trial progress tracking, data collection, and quality control audits.
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