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associated clinical and histological data. Key responsibilities include performing genotyping PCR, isolating biomolecules such as RNA, DNA, and proteins, conducting quality control and concentration
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performing genotyping PCR, isolating biomolecules such as RNA, DNA, and proteins, conducting quality control and concentration assessments, and performing microdissection of tissue samples. The specialist will
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: primary care, acute care, specialty nursing care (sexual health and gynecology), infection control efforts, emergency preparedness, travel medicine, and laboratory services. Oversee and direct the care
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floor resources, oversees orders, billing and expense reporting, plans research-related events, arranges travel and reimbursements, and maintains quality assurance and document control systems in
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rigorous data quality, compliance, and efficient research operations. This role drives the design, implementation, and maintenance of robust data collection and quality‑control processes, supports grant and
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funded “A pilot cluster randomized controlled study (RCT) of “Just ASKTM” to increase cancer clinical trial participations for all patients with breast cancer”. The SHIP Trial seeks to collect research
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regulations, wage tax laws, segregation of duties, DOL, and other federal and state legislation impacting payroll gross-to-net processes; adhere to control objectives established and ensure compliance and
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cloud-based computing environments (e.g., AWS) and version control systems (e.g., Git). Experience in stakeholder engagement, including conducting interviews, facilitating workshops, or synthesizing
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or equivalent combination of education and experience is required. Superb writing and proofreading skills with a strong attention to detail are required Must have an excellent command of language, grammar
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functional groups within the CVPF, including Operations, Manufacturing, Quality Control, Quality Systems, Quality Assurance, and Facilities. The individual will report to the cGMP Operations and Logistics