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The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs. Join us as we continue to grow, the Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes & procedures, and in compliance with FDA, GCP, and ICH regulations and guidelines.
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Working under the supervision of a Senior Research Assistant and Principal Investigator Dr. Lewandowski, and following established policies and procedures, provides assistance on clinical research studies.
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The Clinical Veterinarian will also participate in research support of GLP and non-GLP studies involving both USDcovered and non-covered species; this individual may manage clinical aspects of the studies, provide guidance on animal model and protocol development, and participate on the IACUC through conducting veterinary reviews.
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Overall clinical operations of the facility’s blood cancer research program including enrollment, regulatory, quality, and site operations. Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials.
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Ph. D. in biostatistics or related discipline with 7+ years of experience with patient-reported outcomes, health economics, health technology assessment, and outcomes research methodology used in clinical trials and observational studies.
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The CRC will be responsible for the coordination of complex oncology clinical research protocols, including accurate data collection and overseeing the quality of the clinical trial data and records, scheduling and conducting study initiation and monitoring visits, and participating in ongoing study protocol training.
$43,919 - $67,046 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study.
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Ability to work independently and effectively under a fast-paced and changing environment+ Proficiency Microsoft Office Excel and Outlook+ Able to travel 10% or as neededPreferred Qualifications:+ Real-world data+ Cardiovascular clinical trials+ Electronic data capture (EDC) system (Medidata) and eTMF system (Florence)+ Clinical research certification (i.e., SOCRA, CCRA, CCRC)Click on apply now for instant consideration.
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Preferred: Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) is preferred. Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) certification, along with a minimum of two years additional professional experience, will be considered in place of degree.
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The primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials in cardiovascular and chronic kidney diseases.
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Active partners include investigators at Yale University, Osher Center for Integrative Health jointly based at Brigham and Women's Hospital and Harvard Medical School, The University of Iowa College of Public Health, and RAND Co. The PCCR has excellent clinical research support, including a dedicated research clinic, exceptional clinical research professionals, and an Office of Data Management & Biostatistics.
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This position is part of Clinical Affairs team and will be hybrid to Sunnyvale, CA. The senior clinical research scientist will work on advanced, complex projects requiring state of the art knowledge in oncology and/or infectious disease molecular diagnostics.
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The Senior Clinical Research Scientist develops and independently writes clinical documentation including clinical protocols, clinical study reports and clinical justifications in support of research and new product development, registration and commercialization of products.
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Under the direction of the research principal investigator and manager, the Clinical Research Coordinator I works collaboratively to support hematology, oncology, bone marrow transplant, and cellular therapy clinical trials for pediatric patients.
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The Phase 0 Clinical Trials Navigator will be responsible for reviewing Barrow Brain and Spine neurosurgeon clinics each week to identify individuals who may be clinical trial candidates and performing routine clinical research activities under the direction of the principal investigator, research nurse clinician, and research specialist.
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clinical research jobs Title: quality Company: Pfizer
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