Experienced Clinical Research Associate, Multi-sponsor, France
IQVIA UK
Paris, France
Hybrid
Clinical monitoring visits
Site monitoring visits
Good clinical practice (gcp)
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.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, Case Report Form (CRF) completion and submission, and data query generation and resolution.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
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
Clinical monitoring visits
Site monitoring visits
Good Clinical Practice (GCP)
ICH guidelines
Oncology experience mandatory
Written and verbal communication skills
Nice-to-have
Flexible working hours
Hybrid or home-based role
Problem-solving skills
Effective time management skills
Key Requirements
2 years clinical oncology experience
Bachelor's Degree in scientific discipline or health care preferred
Proficiency in Microsoft Word, Excel and PowerPoint
Good command of English language
Advanced knowledge of applicable clinical research regulatory requirements