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Our research aims to improve quality of life, well-being, symptom and pain management, and reduce caregiver burden:For example, a Clinical Research Coordinator to support a large multi-site clinical trial study that focuses on the comparison of care delivery models to support older adults with complex healthcare needs.
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Responsibilities With direct oversight, the Clinical Authorization Specialist:Manages approval process for clinically complex cases: Discusses complex medical necessity cases in all aspects of the prior authorization work (on-label drug, off-label drug, laboratory testing, and others as assigned) with attending physicians.
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The Principal Scientist, Computational Biology leads the development and deployment of computational methods for NGS-based clinical diagnostic assays in our clinical labs. The successful candidate will have a deep understanding of genomics, cancer biology, and computational biology, and will have a track record of working on cross-functional teams to deliver on complex projects.
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Daily Pay: Work today, get paid today! This is a complex on-property position with Revere Hotel Boston Common and Hyatt Regency Boston Harbor. Ability to access, read and accurately input information using a moderately complex computer system.
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Our projects include but are not limited to clinical trials in addiction, infectious disease, neurology, cardiovascular critical care, novel point-of-care test devices, behavioral health emergencies, advanced care planning, and state-of-the-art digital health innovations such as digital pills, emergency ultrasound, and other novel medical technology.
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Provide technical and clinical instruction of a complex nature during the ultrasound sales and post sale process to internal and external customers, service personnel, including on-site visits to physicians and sonographers.
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Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best-in-class medicines to patients around the world.
$161,600 - $269,400 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Under the general direction of the Charge Nurse or Technical Supervisor, provides ancillary support for clinical activities by performance and appropriate interpretation of simple, moderate, and some highly complex clinical laboratory tests as defined under CLIA '88.
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Leads small and large collaborations with academia and industry partners to identify biobanks, clinical trials and existing databases to collate multi-parameter genomic and clinical datasets to mine for novel biomarkers of unmet need patients in conjunction with computational biologists, data scientists and statistician.
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Keywords : senior director, clinical program lead, late-stage clinical development, clinical trials, global, strategy, hematology, lymphoma, oncology, targeted therapies, ADCs, antibody-drug conjugates, program, asset, label extension, life-cycle management, pharma, biotech, biopharma, MD, medical doctor, phase I, phase II, phase III, FDA.
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Minimum Qualifications:Master’s degree in social work (MSW) from an accredited Clinical Social Work Education (CSWE) program, with emphasis on clinical social work, is required.
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Lead internal and outsourced development and qualification or validation of biomarker assays for clinical trials, applying experience across relevant methods (e.g. qPCR, digital drop PCR, Western blotting), to develop robust assays, generate and analyze data and provide expert interpretation of the effects of promising drug candidates.
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Oversee the planning, implementation, and management of immuno-oncology clinical trials from initiation to completion. The Senior Clinical Trial Manager will play a crucial role in overseeing and managing Phase 1-3 clinical trials related pertaining to mRNA therapies targeting cancer and rare disease.
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Collaborate with the RNA team to conduct in vitro and in vivo studies, leading to eventual clinical trials. Its first product, a differentiated CD47 antibody, has received FDA IND approval in Feb 2023 and will start clinical trial soon.
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HCP include all VA licensed and unlicensed, clinical and administrative, remote and onsite, paid and without compensation, full- and part-time employees, intermittent employees, fee basis employees, VA contractors, researchers, volunteers and health professions trainees (HPTs) who are expected to perform any or all of their work at these facilities.
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complex clinical trials shift work jobs Company: Emory University in Brookline, MA
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