Become part of our team as a Clinical Research Associate II, where you will monitor investigator sites, ensure protocol and regulatory compliance, and manage documentation. This role suits candidates with clinical monitoring experience and a background in life sciences or nursing.
Skills
- clinical monitoring
- ich-gcp compliance
- bachelor's degree in life sciences
- registered nursing certification
- risk based monitoring
- root cause analysis
- sdr
- sdv
- crf review
- clinical trial management system
- investigator site initiation
- trial close out
- medical terminology
- clinical research monitoring
- regulatory compliance
- business writing
- investigator identification
- process improvement
- project reporting
- team collaboration
- presentation skills
- organizational skills
