Clinical Study Associate

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