CRA (Level II)

We are recruiting a Senior 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 experience in clinical research monitoring and strong knowledge of ICH-GCP guidelines.

Skills

• clinical monitoring
• ich-gcp compliance
• risk based monitoring
• sdr
• sdv
• crf review
• root cause analysis
• clinical trial management system
• site management
• regulatory compliance
• problem solving
• critical thinking
• investigational product assessment
• business writing
• investigator site initiation
• trial close out
• essential document management
• presentation skills
• interpersonal skills
• organizational skills
• time management
• process improvement