CRA (Level II)

Monitors investigator sites with a risk-based monitoring approach, applying root cause analysis and problem-solving skills to ensure compliance. Conducts monitoring tasks according to the approved monitoring plan and provides trial status updates to the Clinical Team Manager. Participates in investigator meetings and ensures that essential documents are complete and in place according to ICH-GCP and applicable regulations.

Bachelor's degree in a life sciences related field or Registered Nursing certification. Previous experience as a clinical research monitor (1+ years). Valid driver's license where applicable. Strong understanding of ICH GCPs and applicable regulations.