Clinical Research Associate II

Clinical Research Associate II supporting sponsor-dedicated studies at a global CRO. The role manages site relationships, conducts monitoring visits, ensures regulatory compliance, and maintains clinical documentation across multiple therapeutic areas.

Responsibilities Serve as primary liaison between investigational sites and sponsor Conduct site selection, initiation, monitoring, and closeout visits Ensure site compliance with ICH-GCP, SOPs, and regulatory requirements Monitor patient safety and manage adverse event reporting Resolve data queries and oversee drug accountability Requirements Bachelor's degree in Life Sciences or equivalent, or registered nurse 2+ years of on-site monitoring experience in pharmaceutical or CRO setting Proficiency in ICH-GCP, CTMS, and eTMF systems Monitoring experience across multiple therapeutic areas Eligible to work in US without visa sponsorship Willing to travel 60-75% across southeast region Compensation:

$91,336-$114,170 base