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A clinical research organization is looking for a Quality Control Document Reviewer to join their team! Quality Control Document Reviewer daily tasks. Quality Control Document Reviewer.
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It has direct responsibility for implementing a diverse portfolio of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities, such as a clinical database and biorepository.
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Develop new research topics for advancing geothermal and district heat applications Requirements: Requires a Bachelors, Masters or a PhD in Mechanical Engineering 0-5 years: Thermal fluid system modeling and control background.
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The Research Scientist will be involved directly with the development and execution of clinical and preclinical research goals/activities of CRF. The candidate will work under the direction of the facility manager with respect to the department’s radiochemistry program needs, including routine and novel radiotracer development, production, troubleshooting, and prioritization/facilitation of clinical radiotracer translation.
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The Department of Obstetrics, Gynecology and Reproductive Sciences (Ob, Gyn & RS) is a major academic Department in the School of Medicine, engaged in clinical, research and training activities at the Parnassus, Mt. Zion and San Francisco General Hospital campuses, the Betty Irene Moore Women's Hospital at Mission Bay, as well as satellite locations throughout the Bay Area, with an annual operating budget of $142 million.
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Will also exhibit problem solving skills of a complex nature, participate in Quality Assurance, Quality Control Monitoring, instrumentation maintenance and troubleshooting, specimen processing, phlebotomy, along with customer service.
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Since 1902, Cedars-Sinai has evolved to meet the needs of one of the most diverse regions in the nation, setting standards in quality and innovative patient care, research, teaching and community service.
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The Clinical Supervisor manages research project activities ensuring the quality and integrity of data collection, and trains, manages, and supports student staff and interns, reviewing work products to ensure study protocol is followed as written and approved by the institution’s IRB. This position will assist with the supervision of research coordinators.
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Work effectively in cross-organization environment by collaborating with clinical investigators and industry partners to develop Pathology department support for projects requiring clinical research laboratory testing, including liquid biopsy testing and tissue-based biomarker assays.
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Job Segment: Chemical Research, QC, Six Sigma, Lean Six Sigma, Plant Manager, Engineering, Quality, Management, Manufacturing. As a Quality Leader, you'll be at the forefront of our innovation of having responsibility and accountability for all Quality Control / QMS activities / Quality Systems Support, including but not limited to all SWP (Standard Work Process) activities and responsibilities.
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DBMI has research and/or service programs in the following areas: Clinical informatics, clinical research informatics, bioinformatics, biomedical data modeling and ontologies, biomedical natural language processing and information retrieval, health artificial intelligence and machine learning, privacy technology, global health informatics, equity in informatics, population health informatics, quality informatics, vital records and public health informatics, and translational bioinformatics.
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Works closely with patient, family, and research staff to assure good patient rapport and high-quality clinical care, re-enforcing the desire for patient’s retention in the trial.
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You'll drive work for new applications in research, clinical genomics, and Reproductive Health (RHT). As a Staff Scientist in Clinical NGS, you'll work with a passionate group motivated by science, biology, and their profound impact on human health.
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DPS Group is seeking a qualified Senior Quality Assurance Operations professional to perform batch disposition, batch record review, deviation, CAPA and change control support at the Boston, MA client site.
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Join Takeda as a Research Senior Scientist in Cambridge, MA, where you will act as an e nterprise level partner responsible for the lifecycle management of clinical bioanalytical (PK, ADA) and biomarker samples, data, and specialty lab vendors to maintain chain-of-custody in a GxP-compliant setting.
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clinical research quality control jobs Company: Ucla Health in TX, Us
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