CRA I/II - FSP

Exciting opportunity for a Clinical Research Associate to support oncology and cell therapy clinical trials. Key responsibilities include monitoring investigator sites, ensuring protocol and regulatory compliance, and managing documentation. Ideal for candidates with clinical monitoring experience and a background in life sciences or nursing.

Skills

• clinical monitoring
• ich-gcp compliance
• site management
• risk based monitoring
• root cause analysis
• medical terminology
• regulatory compliance
• clinical trial management system
• on-site monitoring
• remote monitoring
• investigator site initiation
• investigational product assessment
• business writing
• stakeholder management
• presentation skills