Clinical Research Associate

Please submit your application in English

What You'll Do

• Serve as main CTI contact for assigned study sites
• Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory

requirements

• , SOPs and ICH GCP
• Assist with or oversee study start-up activities, including feasibility, pre-study activities and site …