Offer summary
Qualifications:
Minimum five years clinical monitoring experience, Relevant life science degree or equivalent, Strong understanding of Good Clinical Practices, Proficient with Word, Excel, and PowerPoint, In-depth knowledge of drug development processes.
Key responsabilities:
- Monitor investigational sites for compliance
- Manage ongoing study data collection
- Prepare and submit site visit reports
- Support project team with logistical issues
- Establish relationships with sponsors and sites