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IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries. The Clinical Research Associate, Sponsor Dedicated performs site monitoring and management activities, ensuring study sites follow protocols, regulations, guidelines, and sponsor requirements. The role also supports recruitment, regulatory tracking, study documentation, site com

Responsibilities Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals Deliver protocol and study-specific training to site personnel and maintain consistent

This position requires regular on-site work at the location. The role involves coordinating clinical research activities and ensuring compliance with regulatory requirements.

This position requires regular on-site work at Carlsbad, CA. The role involves coordinating clinical research activities and ensuring compliance with regulatory requirements.