This role involves conducting remote or on-site visits to assess protocol and regulatory compliance while managing documentation for top pharmaceutical companies
Job Summary
This role involves conducting remote or on-site visits to assess protocol and regulatory compliance while managing documentation for top pharmaceutical companies.
The successful candidate will apply root cause analysis and critical thinking to identify site process failures and implement corrective actions to ensure data reliability.
Candidates are expected to mentor new team members, assist in preparing project tools, and maintain audit readiness across multiple international sites.
Matching Summary
This role involves conducting remote or on-site visits to assess protocol and regulatory compliance while managing documentation for top pharmaceutical companies.
Skills & Requirements
Must-have
3+ years clinical research monitor experience
Bachelor's degree in life science or nursing
Valid driver's license required
60-80% travel frequency
ICH-GCP and FDA guideline knowledge
Risk-based monitoring application
Nice-to-have
Mentoring junior clinical team members
Root cause analysis skills
Process improvement identification
Collaborative relationship building
Effective presentation skills
Key Requirements
Bachelor's degree in life science or Registered Nursing certification
Minimum 3 years of clinical research monitor experience