Impactful Sponsor‑Dedicated Clinical Research Associate

Benefits

Qualifications

• •Applicants should have at least 2 years of monitoring experience and a Bachelor's degree in a scientific field
• •The role requires strong communication and organizational skills, proficiency in Microsoft Office, and the ability to manage site documents effectively

Responsibilities

• •IQVIA is seeking a Site Monitor in Ontario, California, responsible for conducting site monitoring visits and ensuring compliance with Good Clinical Practice