Clinical Research Associate 2580199 A leading hospital is seeking a skilled Research Associate - Administration. The successful candidate will oversee, manage and participate in research activities. The ideal candidate has 2+ years of experience in a clinical research coordinator role. . The company offers a great work environment! Clinical Research Associate Pay and Benefits: • Hourly pay: $30/hr • Worksite: Leading hospital and health care system (Los Angeles, CA 90020- Job location may require site to site travel - Santa Monica, Torrance) • W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL • 40 hours/week, 3 Month Assignment Clinical Research Associate Responsibilities: • Provide oversight of clinical research sites compliance with ICH/Good Clinical Practices (GCP), governing SOPs (standard operating procedures) and clinical study protocols. • Responsible for research assessment and patient intervention under the supervision of the Principal Investigator. • Responsible for regulatory coordination of clinical research studies, preparation, submission and maintenance of regulatory files to fulfill research requirements. • Additional responsibilities include regulatory compliance, patient recruitment and enrollment, data collection, research chart documentation, quality assurance, report preparation, protocol information dissemination to health care professionals, patients and their family members. • Work may be assigned by Senior Management, and assignments may be changed on an as-needed basis in order to ensure that studies and patient care needs are handled appropriately and in a timely manner. • Travel to other locations may be required. Clinical Research Associate Qualifications: • A multi-tasked individual with a minimum 2 years of experiencein a clinical research coordinator role. • College degree in medicine, science, health, or equivalent. • Performs management of research activities to ensure the collection of accurate clinical data within given timeline. • Knowledge of ICG GCP guidelines and expertise to review, evaluate medical data and all applicable local laws and regulations. • Demonstrated knowledge of all components of the research process as it pertains to clinical trials and studies, i.e., IRB procedures and processes, data management, etc. • Experience in selection and management of vendors/CROs (Central Lab, IVRS, EDC). • Track progress of clinical studies with regard to budget, study milestones, and deadlines.Recruiting & enrolment of patients who meet eligibility criteria, scheduling, completing CRFs. • Able to solve complex problems, prioritize multiple tasks, plan proactively and accomplish goals within project in a dynamic team environment. • Participate in study audits, as applicable. Clinical Research Associate Shift: • Monday-Friday, 8:00-5:00