Clinical Study Associate

Job Summary

A company is looking for a Clinical Study Associate II to support clinical trials management and execution.

Key Responsibilities

• Assist in day-to-day trial execution including site start-up, enrollment, and monitoring
• Prepare and track essential study documents and ensure data quality
• Liaise with CROs and sites, and support investigator/vendor meetings and feasibility assessments

Required Qualifications

• Bachelor's degree in science or higher
• 3+ years of experience in a pharma, CRO, or clinical research environment
• Knowledge of GCP and SOPs, with an understanding of study phases
• Proficient in Word, Excel, and PowerPoint; basic database management skills
• Medical/scientific experience in clinical research is preferred