FSP Bench Clinical Research Associate I

Monitor investigator sites with a risk-based monitoring approach. Ensure data accuracy through SDR, SDV, and CRF review via on-site and remote monitoring activities. Document observations in reports and letters in a timely manner and escalate deficiencies to clinical management. Conduct monitoring tasks according to the approved monitoring plan and maintain regular contact with investigative sites.

Bachelor's degree in a life sciences related field or Registered Nursing certification. Minimal clinical monitoring experience comparable to 2 years in a clinical environment. Knowledge of clinical trials, medical terminology, and health care.