CRA (Level II) to Sr CRA (Level II)

We are currently hiring a Clinical Research Associate (Level II) to support clinical trial monitoring and site management. You will ensure protocol and regulatory compliance, manage documentation, and collaborate with investigational sites. Ideal candidates have at least two years’ experience in clinical research and strong communication skills.

Skills

• clinical trial monitoring
• ich-gcp compliance
• bachelor's degree in life sciences
• registered nursing certification
• medical terminology
• risk based monitoring
• root cause analysis
• clinical research
• site management
• sdr
• sdv
• crf review
• clinical trial management system
• investigational product assessment
• audit readiness
• regulatory documentation
• microsoft office
• business writing
• project tracking
• process improvement
• investigator site initiation
• trial close out
• file review
• stakeholder communication
• team collaboration