RWE Associate Site Manager (French speaker)
Associate Site Manager with French
Real-World Evidence
Hybrid: EMEA
Join us on our exciting journey!
IQVIA Real-World Evidence (RWE) teams work with clients to help them collect and use
- world data to generate evidence to meet the needs of regulators, payers, providers, and patients.
Our approach is unique in the industry and is defining the way companies develop and apply
- world evidence for healthcare decision making.
We are collaborative, intellectually curious, entrepreneurial, and constantly looking for opportunities to harness the value of
- world evidence in an evolving industry.
Due to continued growth, we are seeking new brave minds to join our award winning and innovative department.
Overview
Under the direction and guidance of the Real-World Late Phase Research Clinical Operations Lead, Line Manager or Project Manager, conduct clinical remote monitoring visits and other clinical research activities in accordance with Study Protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (ICH GCP) and applicable regulatory requirements. Gain an understanding of all aspects of Real-World Late Phase Research, Site Management and Site Monitoring.
Responsibilities
- up letters, essential document collection and filing and other required study documentation.
Qualifications
Point.
- solving skills.
- workers, managers and clients and site personnel at assigned sites.
What is in it for you?
- edge
- house technology
JOIN US
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at
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