Clinical Research Associate - Iqvia Biotech (homebased In Paris)
IQVIA Biotech
Paris, France
Site monitoring visits (siv, rmv, cov)
Good clinical practice (gcp) compliance
Subject recruitment plan management
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with GCP and ICH guidelines
Job Summary
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with GCP and ICH guidelines.
Candidates will collaborate with sites to drive subject recruitment plans and manage ongoing project expectations through regular communication.
The position requires maintaining the Investigator's Site File (ISF) and ensuring all study documents are filed correctly in the Trial Master File.
Matching Summary
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with GCP and ICH guidelines.
Skills & Requirements
Must-have
Site monitoring visits (SIV, RMV, COV)
Good Clinical Practice (GCP) compliance
Subject recruitment plan management
Trial Master File (TMF) maintenance
Protocol adherence and data integrity
Nice-to-have
Oncology therapeutic area experience
Strong organizational and problem-solving skills
Effective time and financial management
Proficiency with Microsoft Office suite
Ability to work independently in homebased setting
Key Requirements
Minimum 1 year of monitoring experience
Bachelor's Degree in scientific discipline or healthcare
Background in Life Science, Nursing, Pharmacy, or medical degree