Offer summary
Qualifications:
Bachelor's in life sciences or nursing certification, 2+ years clinical research monitoring experience, Knowledge of medical terminology and therapeutic areas, Understanding of ICH GCPs and regulations, Valid driver's license where applicable.
Key responsabilities:
- Monitor sites with a risk-based approach and troubleshoot issues
- Ensure data accuracy through monitoring and documentation
- Maintain communication with investigative sites for compliance checks
- Contribute to project updates and nomenclature improvements
- Facilitate compliance with protocols and trial management systems