Offer summary
Qualifications:
Bachelor of Science in health-related field or equivalent, 1 year independent clinical monitoring experience, Broad knowledge of medical terminology, Basic knowledge of drug therapy and research methodologies, Comprehensive knowledge of Local Regulations and ICH GCP.
Key responsabilities:
- Conduct pre-study, initiation, monitoring, and closeout visits for research sites
- Perform source document verification, case report form and regulatory document review
- Conduct study drug inventory, adverse event reporting, patient recruitment assessment