Offer summary
Qualifications:
Bachelor’s degree in Life Science or equivalent industry experience, At least 24 months of active monitoring experience, Thorough knowledge of medical terminology.
Key responsabilities:
- Monitor according to Good Clinical Practice guidelines and project protocols
- Complete on-site monitoring within specified timelines
- Attend project and department meetings, submit reports, and ensure site follow-up
- Maintain regular communication with assigned sites and assist with issue resolution
- Assist with training sessions for CRAs and deliver presentations as required