Experienced Clinical Research Associate, Multi-sponsor, France
IQVIA
Paris, France
Hybrid
Conduct clinical monitoring visits
Site monitoring visits
Ensure quality and integrity of study site practices
Conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements
Job Summary
Conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.
Perform site monitoring visits (selection, initiation, monitoring and close out visits) in accordance with contracted scope of work and good clinical practices.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Matching Summary
Conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.
Skills & Requirements
Must-have
Conduct clinical monitoring visits
Site monitoring visits
Ensure quality and integrity of study site practices
Manage study progress
Maintain Investigator's Site File
Good Clinical Practice (GCP)
International Conference on Harmonization (ICH)
Nice-to-have
Flexible working hours
Hybrid or home-based role
Collaborate and liaise with study team members
Key Requirements
Bachelor's Degree in scientific discipline or health care preferred
2 years clinical oncology experience mandatory
Proficiency in Microsoft Word, Excel and PowerPoint