We are seeking a Clinical Research Associate (Level II) to support clinical trial monitoring and site management in Sweden. You will ensure protocol and regulatory compliance, manage documentation, and collaborate with investigational sites. Ideal candidates have experience in clinical research monitoring and strong communication skills.
Skills
- clinical monitoring
- ich-gcp compliance
- bachelor's degree in life sciences
- clinical research monitoring
- risk based monitoring
- root cause analysis
- sdr
- sdv
- crf review
- regulatory compliance
- clinical trial management system
- investigational product assessment
- site initiation
- trial close out
- medical terminology
- clinical trial site management
- investigator site management
- business writing
- project team collaboration
- presentation skills
- microsoft office
- process improvement
- fluent swedish
