You will conduct remote or on-site visits to assess protocol and regulatory compliance while managing required documentation across global clinical trials
Job Summary
You will conduct remote or on-site visits to assess protocol and regulatory compliance while managing required documentation across global clinical trials.
The role requires applying root cause analysis and critical thinking to identify site process failures and implement corrective actions to ensure data reliability.
As a Level II associate, you will manage procedures from various sponsors and serve as a site processes specialist to guarantee subject rights and well-being.
Matching Summary
You will conduct remote or on-site visits to assess protocol and regulatory compliance while managing required documentation across global clinical trials.
Skills & Requirements
Must-have
Bachelor's degree in life sciences
1 year clinical research monitor experience
Valid driver's license
ICH-GCP guidelines knowledge
Risk-based monitoring approach
Root cause analysis skills
Nice-to-have
Oncology study experience
HIV or COPD study experience
Strong business writing standards
Collaborative team relationship building
Process improvement contributions
Key Requirements
Bachelor's degree in life sciences or nursing certification
1 year experience as a clinical research monitor
Completion of PPD Drug Development Fellowship (alternative)