Seeking a Clinical Research Associate (Level II) to support clinical trial monitoring and site management. Key responsibilities include ensuring protocol and regulatory compliance, managing documentation, and collaborating with investigational sites. Ideal for candidates with clinical research experience and strong monitoring skills.
Skills
- clinical monitoring
- ich-gcp compliance
- oncology clinical research
- risk based monitoring
- cell therapy clinical research
- root cause analysis
- sdr
- sdv
- crf review
- clinical trial management system
- regulatory documentation
- site initiation
- site close out
- investigational product assessment
- medical terminology
- clinical research monitoring
- business writing
- problem solving
- critical thinking
- investigator identification
- project status reporting
- process improvement
- team collaboration
