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.
This position requires frequent travel of 60-80% to investigate sites, participate in investigator meetings, and maintain audit readiness across multiple countries.
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
Bachelor's degree in life sciences
1 year clinical research monitor experience
Valid driver's license where applicable
ICH-GCP guidelines knowledge
Risk-based monitoring concepts
Critical thinking and problem solving
Nice-to-have
Excellent oral and written communication skills
Ability to work independently or in a team
Strong organizational and time management skills
Experience with Clinical Trial Management Systems
Good presentation skills
Key Requirements
Bachelor's degree in life sciences or Registered Nursing certification
1 year experience as a clinical research monitor
Completion of PPD Drug Development Fellowship (alternative)