Clinical Research Associate - Sponsor Dedicated

IQVIA seeks experienced Clinical Research Associates II and Senior Clinical Research Associates to oversee clinical trial sites across multiple therapeutic areas nationwide. The role involves managing all phases of site monitoring, ensuring protocol compliance, regulatory adherence, and quality standards while supporting study enrollment and data integrity.

Responsibilities Conduct site selection, initiation, routine monitoring, and close-out visit activities Evaluate site performance and ensure protocol adherence, GCP compliance, and regulatory requirements Partner with investigative sites on patient recruitment and retention strategies Deliver protocol training and maintain ongoing communication with site staff Monitor study progress, track enrollment metrics, and resolve data queries Requirements Bachelor's degree in Life Sciences, Healthcare, Nursing, or related field preferred Minimum 2 years of independent on-site monitoring experience in pharmaceutical, biotech, or CRO industry Strong understanding of clinical research processes, GCP, and ICH guidelines Proficiency with Microsoft Office and electronic data capture technologies Excellent verbal and written communication skills Strong organizational and time management abilities Ability to work independently and collaboratively across multiple priorities Compensation:

$74,500.00 - $197,500.00 base