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Health Wealth Safe is hiring a Clinical Research Associate II to conduct on-site monitoring of clinical trials across multiple therapeutic areas. The role oversees site visits, compliance, study progress, and collaboration with investigative sites and cross-functional teams. Responsibilities Site selection, initiation, monitoring, and closeout visits in compliance with GCP and regulatory standards Building relationsh

Lexitas Pharma Services is an ophthalmic product development organization seeking a Biostatistician to support the design, collection, analysis, reporting, interpretation, and publication of clinical trial data. The role contributes to statistical methodology, validates clinical trial endpoints and datasets, collaborates with stakeholders, and ensures the integrity and compliance of statistical deliverables. Responsi

FSP Clinical Research Associate 2 - West Coast - Oncology & Non-Oncology jobs in United States Tags 50+ applicants Original Job Post Fortrea +11 more $100K/yr - $112K/yr 97 STRONG MATCH Experience Level 100 Skill Industry Exp. 90 Responsibilities Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initi

IQVIA is a global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries. The Clinical Research Associate II conducts independent on-site monitoring activities, supports investigative sites, tracks study progress and compliance, maintains trial documentation, and collaborates with cross-functional teams to deliver clinical studies succe

Duke University is an academic medical center conducting interdisciplinary biomedical and clinical research through Duke Health and its School of Medicine. The Clinical Research Coordinator will support or lead day-to-day operations of clinical research studies in Gastroenterology, including participant recruitment and consent, study visits, regulatory documentation, specimen management, data collection, and collabor

This position involves independently managing multiple oncology clinical trials from startup through closeout while serving as the primary point of contact between patients, physicians, sponsors, research staff, and clinical teams. • Coordinate all phases of clinical trials, including activation, enrollment, conduct, monitoring, and study closure.