CLINICAL RESEARCH ASSOCIATE - IMM/CROSS TA - SOUTHERN CALIFORNIA (FIELD BASED)

As a clinical research associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. what you will be doing: serve as the primary point of contact between investigational sites and the sponsor conduct all types of site visits, including selection, initiation, routine monitoring, and close-out ensure site compliance with ich-gcp, sops, and regulations maintain up-to-date documentation in ctms and etmf systems support and track site staff training and maintain compliance records monitor patient safety, ensuring timely and accurate ae/sae/pqc reporting support subject recruitment and retention efforts at the site level oversee drug accountability and ensure proper storage, return, or destruction resolve data queries and drive timely, high-quality data entry document site progress and escalate risks or issues to the clinical team assist in tracking site budgets and ensuring timely site payments (as applicable) collaborating with cross-functional partners including ctas, ltms, and ctms you are: a graduate with a bachelor’s degree in life sciences or equivalent, or a qualified rn eligible to work in united states without visa sponsorship a clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or cro industry experienced across multiple therapeutic areas, including immunology preferred. proficient in ich-gcp, local regulatory requirements, and clinical systems like ctms and etmf a clear communicator, problem-solver, and collaborative team player willing an...