Study Coordinator
Job Summary
Residing in or near Buenos Aires, Argentina, the part-time Study Coordinator will manage remote site activities for assigned projects, serving as the primary contact for communications and supporting recruitment and protocol activities.
Key responsibilities
- Coordinate day-to-day site communications, document submissions, and activity management
- Assist with subject re-consenting, medical record acquisition, and protocol activities as directed by the Principal Investigator
- Perform data entry, monitor clinical databases, and maintain documentation in compliance with IRB/FDA policies
Required qualifications
- Bachelor's degree or equivalent experience with a minimum of 2 years of related experience
- Current knowledge of ICH/GCP and applicable regulations and guidelines
- Experience with technology and web-based research platforms
- Strong organizational skills and ability to multitask
- Ability to work independently and collaboratively with other team members
Complete Job Description
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