Offer summary
Qualifications:
Bachelor's degree in life sciences or equivalent certification, Minimal clinical monitoring experience (around 2 years), Basic knowledge of medical terminology and ICH GCPs, Good verbal and written communication skills, Proficient in Microsoft Office and digital tools.
Key responsabilities:
- Perform and coordinate clinical monitoring and site management.
- Conduct on-site and remote visits for compliance assessment.
- Manage documentation and regulatory requirements effectively.
- Ensure data accuracy, and monitor investigator sites.
- Maintain ongoing communication with investigative sites.