Experienced Clinical Research Associate, Iqvia Biotech - Home Based, Italy
IQVIA Inc
Italy
Good clinical practice (gcp) compliance
International conference on harmonization guidelines
Site monitoring visit execution
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with regulatory requirements
Job Summary
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with regulatory requirements.
Candidates will work with sites to adapt and drive subject recruitment plans to enhance predictability and project success.
The position requires maintaining the Investigator's Site File and ensuring all study documents are available for filing in the Trial Master File.
Matching Summary
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with regulatory requirements.
Skills & Requirements
Must-have
Good Clinical Practice (GCP) compliance
International Conference on Harmonization guidelines
Site monitoring visit execution
Subject recruitment plan management
Trial Master File maintenance
Nice-to-have
Strong problem-solving skills
Effective client relationship building
Flexibility to travel within Italy
Excellent command of English language
Key Requirements
University Bachelor's Degree in scientific discipline or health care
Master's Degree in scientific discipline or health care
CRA Certification as required by Ministerial Decree dated 15.11.2011
Experience in Pharma Industry and/or Clinical Trials environment