Clinical Trials Coordinator II - Hybrid Data & Compliance in Reading

Clinical Trials Coordinator II - Hybrid Data & Compliance in Reading

Reading Full-Time No working from home possible
IQVIA Argentina

IQVIA Argentina is seeking a Clinical Trials Assistant based in Reading, United Kingdom. This role involves supporting Local Trial Managers and Clinical Research Associates in managing clinical trials effectively. Key responsibilities include tracking trial progress, managing study data, and ensuring documentation compliance.

The ideal candidate will have a degree in life sciences and prior experience as a CTA, along with proficiency in Microsoft Office tools. Strong communication and organizational skills are essential for success in this role.

#J-18808-Ljbffr
IQVIA Argentina

Contact Details:

IQVIA Argentina Recruitment Team