Offer summary
Qualifications:
Minimum 1 year of clinical trials experience, M.A/M.Sc degree in medical/bioscience, Strong IT skills and data analysis capability, Fluent in English and local language, Good understanding of ICH-GCP and regulations.Key responsabilities:
- Act as primary site contact and manager
- Conduct various site monitoring visits
- Ensure compliance with protocols and regulations
- Communicate with investigators on site issues
- Manage clinical trial systems effectively