Bachelor's degree in life sciences or nursing certification
2 years clinical monitoring experience
Valid driver's license required
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 frequent travel (60-80%) to investigate sites, maintain audit readiness, and collaborate with sponsors 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 or nursing certification
2 years clinical monitoring experience
Valid driver's license required
Knowledge of ICH-GCP guidelines and regulations
Risk-based monitoring approach application
Nice-to-have
Strong critical thinking and problem-solving skills
Excellent oral and written communication abilities
Ability to work independently and in teams
Flexibility to adapt to various scenarios
Experience with Clinical Trial Management Systems
Key Requirements
Bachelor's degree in life sciences or Registered Nursing