Senior Clinical Research Associate Ii (Lead Monitor) (Santiago)

You will

• Facilitate regional projects as Lead Monitor and supervise study activities, timelines and schedules
• Train Monitors in annotated monitoring visit reports
• Review monitoring reports and support monitors in their activities
• Act as the main communication line between Monitor and Regional Lead
• Facilitate site budgets and contract negotiations
• Be a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress and lead project team calls on the country level
• Participate in quality control and compliance monitoring
• May need to monitor and manage sites (if applicable)
• May need to supervise monitors on site
• Oversee and maintain study‑specific and corporate tracking systems at site and country level

Qualifications

• College/University degree in Life Sciences, Pharmacy, RN or an equivalent comb...