247 parallel-processing-bioinformatics "https:" positions at Boston Children's Hospital
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experience, preferably in cardiology or inherited disease research. Demonstrated knowledge of Good Clinical Practice (GCP), research ethics, and IRB processes. Proficiency in medical record systems (e.g., Epic
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coordination, and customer service. This role manages clinic activity, resolves scheduling and service issues, handles calls and authorizations, and contributes to training and process improvement initiatives
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for presentations to stakeholders. Supports the annual planning and goal setting process by participating in the development of the plan, conducting the appropriate business analytics, competitive
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area/modality. Collects, verifies, records and processes patient demographics, insurance/payment and referral information required for patient appointments in accordance with HIPAA approved procedures
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: 150616512 General Summary Performs specimen processing, computer order entry, evaluation of specimen integrity and pre analytical processing. Provides customer service through answering inquires regarding
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(OR), Post-Anesthesia Care Unit (PACU), and Day Surgery. Key functions include monitoring inventory levels, restocking supplies, and adjusting par levels as needed to meet surgical demand. The team handles
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scientist, you will engage in a variety of routine and specialized clinical data analyses, biobank specimen preparation and sample processing, laboratory studies on patient-related samples, and statistical
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ongoing support during admission for all families Supportive counseling as families process and cope with medical diagnoses Develop and maintain effective therapeutic relationships with patients and
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organizational initiatives & projects with a focus on continuous process improvement. Performs various administrative functions requiring basic knowledge of programs and services. Key Responsibilities: Provides
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with clinical teams, label, process, and ship biospecimens to collaborating laboratories following study SOPs. Assist with IRB submissions, regulatory documents, continuing reviews, and protocol