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 must apply root cause analysis and problem-solving skills to identify site process failures and implement corrective actions to ensure data accuracy.
This position requires frequent travel of 60-80% to investigate sites, participate in investigator meetings, and maintain audit readiness across central Poland.
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
3 years total CRA experience
2 years on-site oncology experience
Bachelor's degree in life science
Risk-based monitoring approach
ICH-GCP guidelines knowledge
Valid driver's license
Nice-to-have
Strong critical thinking skills
Effective communication abilities
Root cause analysis expertise
Collaborative team mindset
Adaptability to travel demands
Key Requirements
Bachelor's degree in life science or nursing certification
Minimum 3 years total experience as a CRA
At least 2 years of on-site hands-on oncology experience