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The Clinical Lab Scientist 1, under general supervision, operates specialized instruments to conduct clinical lab tests and analyze data from results, to assist physicians with diagnosing medical conditions.
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Then you might be a great fit for a Data Research Analyst role with DaVita Clinical Research (DCR) We are looking for a highly motivated, positive and innovative Data Research Analyst to help support our Outcomes Research Data Services Team. The individual will be responsible for utilizing existing SQL scripts to aggregate data for internal and external customers, modifying existing code as needed, documenting projects and procedures, performing quality control, and other tasks as directed.
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NCH is transforming into an Advanced Community Healthcare System(TM) and we’re proud to: Provide higher acuity care and Centers of Excellence; Offer Graduate Medical Education and fellowships; Have endowed chairs; Conduct research and participate in national clinical trials; and partner with other health market leaders, like Hospital for Special Surgery, Encompass, and ProScan.
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Oversees clinical research studies, collecting all clinical data in an accurate and timely manner. · 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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JOB SUMMARYThe Research RN, NCHRI works directly with the physician in accurately and professionally executing all clinical research projects in an acute care/inpatient setting (ED, Cath Lab, ICU, EP lab, Step down and OR) as well as the ambulatory and ancillary areas.
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The Research RN must possess the knowledge and clinical experience to work in many different areas with numerous teams in order to experience success in this position. · Serves as an internal and external resource for questions referencing clinical research at NCH. · Professionally represents Principal Investigator and NCH Research Institute at protocol meetings and conference calls in the absence of the Investigator.
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Coordinates critical research tasks and patient activities in accordance with Good Clinical Practice (GCP). · Assures all data points are supported by medical records, physician notes, diagnostic reports, procedural summaries, or research project documents.
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Represents the Research Institute in a professional manner, demonstrating knowledge and enthusiasm for clinical research. This position manages the research related care of these patients, assists in project initiation, facilitates patient enrollment, encourages patient retention in trials, reports to sponsors on progress/status, and coordinates study participation with other clinical care plans.
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Serves as the contact for physicians and other caregivers in assuring all research and related clinical needs are met. · Performs required procedures and data collection activities at necessary in observational settings such as, ED, Cath Lab, EP Lab, ICU/Step down area, physician office, OR, and other required areas.
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Protocol driven research tasks performed by the physician are guided by the Research Nurse to assure all required steps are completed and performed in the correct order. · Guides referring physicians in GCP compliance and clinical care through protocol design and awareness through education.
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Serves as the primary clinical trial contact person for study sponsor, patient, family, or other healthcare contacts or departments. · Works with sponsor’s auditor/monitor to review and verify accuracy and completeness of data recorded.
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Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it.
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Bachelor's Degree in a related field and 6+ years of related work experience (including data analytics, data management, health economics, medical affairs, clinical risk, clinical trial operations, clinical safety, quality assurance or regulatory affairs) OR advanced degree (PhD, research-based MS, MD, RN/DVM) in a related field with 4+ years of related work experience.
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The Research Associate Clinical I-Data Manager will help the study team in preparing for monitoring visits and audits and ensure compliance with all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board ( IRB.
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Ambulatory, acute & post-acute quality, clinical performance, and operations reporting & analysis. This position supports data quality and data stewardship functions to maintain data accuracy and identify new metrics.
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clinical research data quality market jobs Company: Biospace in TX, Us
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