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programming with SQL, Python, R and/or SAS is required. Experience with semi-structured/unstructured data environments, machine learning, and natural language processing (NLP) desired. Experience with clinical
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range for this role when Hired for NYC Offices Position Summary Responsible for manufacturing and performing quality control (QC) tests of gene therapy products in compliance with the quality system
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time. Maintains calendars by balancing competing priorities and requests for maximum productivity. Oversees travel arrangements for the Chair and designated visitors. Organizes conference calls/meetings
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of equipment, products and experimental techniques. Responsible for tissue & cell culture activities. May run routine biochemistry assays including western blotting and RT-PCR. Audits and screens vendors
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and ICD10 CM coding guidelines. Ability to meet productivity standards and identify any issues or trends and bring them to the attention of management. Demonstrated ability to function independently and
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of hazardous material waste and wet tissues utilizing established protocols. Monitors and maintains schedules and usage of necropsy suite to ensure proper protocols are followed. Assists with training
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office training, developmental and productivity sessions may be required. Ability to work independently and maintain confidential and professional relationships with a variety of personnel. Knowledge
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, ensuring to meet productivity and quality-based departmental benchmarks. Performs charge entry batch quality assurance. Reviews and resolves charge router and charge review edits, as needed. Submits queries
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, chemotherapy, TPN, investigational drugs and other sterile products and extemporaneous preparations. If applicable, completes written records of dispensing for all medication including controlled substances and
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sensitive nature on a daily basis. Coordinates calendars and schedules appointments and meetings. Prioritizes requests for meetings and coordinates the necessary arrangements for meetings. Coordinates