Offer summary
Qualifications:
Bachelor's degree in life sciences or registered nursing certification., Minimal clinical monitoring experience (comparable to 2 years)., Basic medical and therapeutic area knowledge., Understanding of ICH GCPs and applicable regulations., Good command of English language..
Key responsabilities:
- Monitors investigator sites for compliance.
- Conducts on-site and remote visits.
- Documents findings and escalates issues.
- Initiates clinical trial sites as per protocol.
- Contributes to project publications and improvements.