Clinical Study Associate

Job Summary

A company is looking for a Clinical Study Associate to support the execution of clinical trials.

Key Responsibilities:

• Assist in trial execution, including site start-up, enrollment, monitoring, and data flow management
• Prepare essential study documents and track accuracy in the Trial Master File (TMF)
• Collaborate with CROs and sites on sample handling, monitor patient status, and manage lab schedules

Required Qualifications:

• Experience in a pharmaceutical, CRO, or clinical research setting
• Familiarity with GCP guidelines, SOPs, and clinical study phases
• Proficiency in Microsoft Word, Excel, PowerPoint, and basic database management
• Medical-scientific experience in clinical research is preferred
• Experience in monitoring, study coordination, or data handling is preferred