Offer summary
Qualifications:
Bachelor's degree in life sciences or equivalent, Minimal clinical monitoring experience (equivalent to 2 years), Understanding of medical terminology, Knowledge of ICH GCPs and applicable regulations, Good English language proficiency.
Key responsabilities:
- Conduct site monitoring and ensure compliance
- Document findings and manage issues expediently
- Facilitate communication between teams and sites
- Assist in investigator selection and trial startup
- Submit project status tracking and update reports