This role involves conducting remote or on-site visits to assess protocol and regulatory compliance while managing documentation for clinical trials
Job Summary
This role involves conducting remote or on-site visits to assess protocol and regulatory compliance while managing documentation for clinical trials.
Candidates will apply risk-based monitoring approaches to identify site process failures and implement corrective actions to ensure data accuracy.
The position offers a comprehensive benefits package including medical plans, paid time off, parental leave, and a competitive 401(k) retirement plan.
Matching Summary
This role involves conducting remote or on-site visits to assess protocol and regulatory compliance while managing documentation for clinical trials.
Salary
Base: $82,800.00–$154,613.00 (Nevada); Bonus: Variable annual bonus based on performance; Benefits: Comprehensive total rewards including medical, dental, vision, PTO, and 401(k)
Skills & Requirements
Must-have
2+ years clinical research monitor experience
Bachelor's degree in life sciences or nursing
Valid driver's license required
60-80% travel frequency
ICH-GCP and protocol compliance knowledge
Nice-to-have
Risk-based monitoring approach expertise
Root cause analysis and problem solving skills
Excellent written and oral communication
Experience with Clinical Trial Management Systems
Collaborative team relationship building
Key Requirements
Bachelor's degree in life sciences or Registered Nursing certification
Minimum 2 years of experience as a clinical research monitor