Sr CRA (Level I) for FSP

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. Ensures essential documents are complete and conducts on-site file reviews as per project specifications.

Bachelor's degree in a life sciences related field or Registered Nursing certification. Previous experience comparable to 2+ years as a clinical research monitor. Valid driver's license where applicable.