The role involves conducting remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for clinical trials
Job Summary
The role involves conducting remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for clinical trials.
Candidates will apply root cause analysis and critical thinking to identify site process failures and implement corrective actions to ensure data reliability.
The position requires maintaining audit readiness and developing collaborative relationships with investigational sites across various global environments.
Matching Summary
The role involves conducting remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for clinical trials.
Skills & Requirements
Must-have
Risk-based monitoring approach
ICH-GCP guidelines compliance
Root cause analysis skills
On-site and remote monitoring
Protocol and regulatory adherence
Nice-to-have
Critical thinking and problem solving
Collaborative relationship building
Effective oral and written communication
Adaptability in diverse scenarios
Process improvement contributions
Key Requirements
Bachelor's degree in life sciences or nursing certification