Job Description

**Research Assistant**

**Work Setup:** On-site
**Scheduled Weekly Hours:** 24

**Job Summary**

We are seeking a **highly organized and detail‑driven Research Assistant** to support clinical trial operations in accordance with regulatory, ethical, and organizational standards. This position plays an important role in ensuring data accuracy, participant safety, and smooth study execution. The ideal candidate brings strong critical thinking skills, adaptability in a fast‑paced environment, and exceptional communication and teamwork abilities.

**Key Responsibilities**

+ Perform accurate **EDC data entry** , manage queries, and ensure timely resolution.
+ Maintain and update the **regulatory binder** in compliance with documentation and audit standards.
+ Coordinate and schedule **subject visits, procedures, and follow-up activities** .
+ Build effective working relationships with investigators, clinical staff, and study team m...

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