Clinical Study Coordinator

Há 11 horas


São Paulo, São Paulo, Brasil beBeeStudy Tempo inteiro R$44.423 - R$65.491
Job Description

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
Benefits

This is a developmental role that offers extensive training and opportunities for growth.

Others

The 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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