Coordinating CRA - São Paulo
há 1 semana
Job summary
Perform monitoring and site management work for various protocols. Manage site visit schedules, track subject recruitment plans, administer protocol training, evaluate study site practices.Qualifications
- Bachelor's Degree in scientific discipline or health care preferred;
- At least 4 years of on-site monitoring experience;
- In-depth knowledge of clinical research regulatory requirements (GCP and ICH guidelines);
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