Sr CRA (Level I)

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. A minimum of 3 years of completed on-site clinical monitoring experience. Preferred experience in infectious disease, respiratory, ophthalmology, and oncology clinical studies.