临床研究员

Responsibilities

• Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas; - Perform source document verification and case report form review; - Perform regulatory document review; - Conduct study drug inventory; - Perform adverse event and serious adverse event reporting and follow-up; and - Assess patient recruitment and retention.

Qualifications

• Bachelor of Science in health-related field (a BSN is preferred); - Min. 2 years of proven CRA experience; - Broad knowledge of medical terminology and clinical patient management; - Basic knowledge of drug therapy techniques and clinical research methodologies; - Fluency in local language and excellent English. **This is a fully remote-based role.