FSP Sr Clinical Research Associate

Monitors investigator sites with a risk-based monitoring approach. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Documents observations in reports and letters in a timely manner using approved business writing standards. Conducts monitoring tasks in accordance with the approved monitoring plan.

Bachelor's degree in a life sciences related field or a Registered Nursing certification. Previous experience comparable to 2+ years as a clinical research monitor. Effective clinical monitoring skills and demonstrated understanding of ICH GCPs.