Qualifications
Required:
•Bachelor degree in chemistry, biology, nursing or other related field.
•Demonstrated working knowledge of current medical terminology specific to oncology, to accurately read entries in patient charts, and record accurate and timely information into study records and other appropriate research data forms.
•Clinical research experience, with in-depth knowledge of clinical oncology as it pertains to clinical trials.
•Demonstrated experience submitting IND and correspondences with the FDA.
•Working knowledge of “Good Clinical Practices,” as defined by the FDA.
•Demonstrated organizational skills to efficiently and effectively provide data management/monitoring support for multiple clinical trials and projects, providing accurate information in a timely manner.
•Demonstrated experience working with Electronic Medical Record (EMR) systems such as Epic, Cerner, etc.
•Ability to work in a fast-paced environment and to shift priorities to meet deadlines.
•Willingness to travel between UCLA Westwood and Santa Monica Clinic.
•Ability to work with a high level of accuracy especially when preparing lab specimens for shipment and/or delivery to clinical research laboratories.
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