Offer summary
Qualifications:
Bachelor’s degree in science or health-related discipline, 7 years industry experience or equivalent, 5 years clinical research experience, including site monitoring, 3 years recent oncology clinical trial experience, Strong knowledge of regulatory compliance and methodology.
Key responsabilities:
- Monitor clinical trials and manage sites
- Travel up to 80% within assigned territory
- Communicate with study staff and report findings
- Assist with audit preparations and investigator meetings
- Collaborate with the project team and field monitor