Senior Study Coordinator

ResponsibilitiesProvide key support to life-changing clinical research. Become part of a dynamic, world-class health provider. Elevate and achieve your professional potential. You can do all this and more at UCLA Health.Under the guidance of the Director of Clinical Research, we're looking to you to manage the logistical and administrative aspects of clinical research studies. Working closely with faculty principal investigators, you'll serve as study coordinator across all assigned imaging research programs. You'll collaborate with modality directors/managers, contracts, grants management and other departments to ensure compliance, safety and ethical conduct of clinical research trials.QualificationsWe're seeking a flexible, self-motivated professional with a related Bachelor's degree or equivalent clinical research or analytical experience. You must also have:Ability to analyze information, problems, situations and procedures to define objectives, identify patterns and formulate conclusions.Strong communication, interpersonal, organizational, prioritizing and time-management skills.Previous experience managing clinical trials in university setting with exposure to state and federal regulations.Knowledge of the preparation of research regulatory documents, informed consents, and IRB submissions.Experience in data management of clinical research protocols.Knowledge of FDA regulations, ICH guidelines and Good Clinical Practice.Knowledge of medical terminology.Preferred ACRP or SoCRA certification. Computer proficiency.UCLA Health is a world-renowned health system with four award-winning hospitals and dozens of primary care practices, specialty practices, urgent care centers and other ancillary locations throughout metro Los Angeles. Through the efforts of our outstanding people, we have become Los Angeles' trusted provider of exceptional, compassionate patient care. If you're looking to experience greater challenge and fulfillment in your career, you can at UCLA Health.
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