You will conduct remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for clinical trials
Job Summary
You will conduct remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for clinical trials.
The role requires applying a risk-based monitoring approach with root cause analysis to identify site process failures and implement corrective actions.
As part of a global team supporting top pharmaceutical companies, you will ensure audit readiness and maintain collaborative relationships with investigational sites.
Matching Summary
You will conduct remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for clinical trials.