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, appropriate supplies maintained, secured and disposed of according to established policies and procedures. 3. Performs intubation, mechanical ventilation, vascular catheterization and line placement for
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Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines. May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with
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to sponsor’ inquiries regarding protocol start-up activities and recruitment. Performs literature reviews. Qualifications Education: High School Diploma/GED, required. Bachelor's degree in a Science, Sociology
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, and analysis and operation and maintenance of specialized equipment. Knowledge of safety standards and maintenance of specialized equipment. About Us Cedars-Sinai is a leader in providing high-quality
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. This includes performing data searches and other related administrative tasks. Processes clinical data using a range of computer applications and database systems to support cleaning and management of subject or
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for programs with growth potential. Identifies, pursues, and secures opportunities for research program development and growth. Evaluates and optimizes clinical research staff performance, compliance
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reside in the commutable area. The Clinical Research Associate I works under the direction of a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff
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will perform a variety of routine experimental protocols and procedures to support the objectives of one or more laboratory research projects in a specific area of research. The RA I team member will be
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works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures
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using a range of computer applications and database systems to support cleaning and management of subject or patient data. Produces project reports. Performs data searches and other related administrative