This role involves conducting remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for clinical trials
Job Summary
This role involves conducting remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for clinical trials.
The position requires applying root cause analysis and critical thinking to identify site process failures and implement corrective actions to ensure data reliability.
Candidates must possess good Norwegian language skills alongside English proficiency to effectively communicate with investigative sites and internal teams.
Matching Summary
This 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
2 years clinical monitoring experience
Valid driver's license
ICH-GCP guidelines knowledge
Risk-based monitoring approach
Norwegian language skills
Nice-to-have
Root cause analysis skills
Critical thinking abilities
Collaborative relationship building
Process improvement mindset
Flexible and adaptable work style
Key Requirements
Bachelor's degree in life sciences or nursing certification