FSP - CRA (Level I)

Monitor investigator sites using a risk-based approach and conduct root cause analysis to identify failures. Ensure data accuracy through reviews and document observations in reports. Maintain communication with investigative sites to confirm protocol adherence and resolve issues. Participate in investigator meetings and assist in the clinical trial site initiation process.

Bachelor's degree in a relevant field. Familiarity with ICH GCP regulations and clinical trial processes. Strong analytical skills and ability to conduct monitoring tasks independently. Experience in clinical research is preferred.