- Seoul, Seoul, South Korea
- Hybrid
- Entry
- 0–2 years
Monitors patient data and study-related information at clinical trial sites, ensuring compliance with protocols and regulations.
Responsibilities
- Act as frontline liaison between Novartis and study sites
- Manage assigned study sites and conduct phase I-IV protocols
- Perform Site Initiation Visits and ongoing training
- Conduct continuous site monitoring activities (onsite and remote)
- Document and ensure compliance with GCP, ICH, and local regulations
Requirements
- Degree in scientific or healthcare discipline (or 4-year degree plus relevant healthcare experience in the United States)
- Nice to have: clinical study reports
- Nice to have: clinical trials monitoring
- Nice to have: collaboration
- Nice to have: data integrity