IQVIA UK seeks experienced Clinical Research Associates to join our cFSP sponsor-dedicated team in Reading. You will perform site monitoring visits and ensure GCP/ICH compliance while maintaining strong site relationships.
With at least 2 years of on-site monitoring, you will drive subject recruitment plans, deliver protocol training, and coordinate regulatory submissions. This full-time role offers cross-functional collaboration in a fast-paced environment.
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Clinical Research Associate II - Flexible, Impactful Role in Reading employer: IQVIA Argentina
IQVIA is an excellent employer that fosters a collaborative and innovative work culture, providing its employees with the opportunity to grow professionally while working on impactful financial reporting across Europe. With a strong emphasis on employee development and proficiency in leading financial systems like PeopleSoft and SAP, team members can expect meaningful career advancement in a supportive environment that values integrity and excellence.
