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The Oncology Research Nurse Practitioner I is an Adult Nurse Practitioner who manages the direct care of patients enrolled in clinical trials within the Herbert Irving Comprehensive Cancer Center at Columbia University Medical Center.
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A Senior Research Scientist that specializes in organ transplantation and social behavioral science, chronic disease will work mostly with primary data collected through large multi-site studies and clinical trials in support of NIH and DoD funded research.
$150,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Under guidance from the investigators, the Research Nurse Practitioner supervises and coordinates clinical research trials. East Side 525 Clinical Trials. Major clinical research projects investigate antimicrobial drug resistance, hepatitis, HIV/AIDS, hospital epidemiology/infection control, human papillomavirus, respiratory viruses, and transplantation/oncology ID.
$156,000 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Divisional faculty are actively engaged in a diverse array of funded research programs spanning basic and translational research into the pathogenesis of kidney diseases, epidemiology, and clinical trials to improve the care of patients with kidney disease.
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Review Beacon Build Template as completed by Physician Investigator for all trial patients enrolled onto clinical trials with assigned DMG. Ensure treatment plan is correctly built into Beacon Build Template.
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Reporting to the Director of Clinical Research Operations, provide support, establish workflows and processes for high-quality clinical research activities for various Oncology Phase 2 through 4 trials.
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Research Assistant I The Research Assistant will be responsible for assisting the clinical research staff in conducting clinical research trials. KNOWLEDGE & EXPERIENCE Education: High school diploma or equivalent required Experience: Prior experience in clinical research is not required but preferred Credentials: Phlebotomist certificate preferred Medical Assistant Certification preferred Knowledge & Skills: Knowledge of medical terminology required Must be detail-oriented and demonstrate attention to detail Excellent customer service skills Excellent computer skills Powered by JazzHR.
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The Registered Nurse assists the Investigators in executing Phase I, II, III, and IV clinical research trials in accordance with Standard Operating Procedures (SOPs), FDA and GCP guidelines, and study protocols.
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As the Clinical Research Monitor, you will ensure trial patients' safety by assuring trials are conducted ethically and within regulatory compliance, data accuracy, and protocol adherence.
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Overview: Under the direction of the Principal Investigator (PI), the Clinical Research Assistant (CRA) will coordinate and oversee all activities of multiple Pediatric Oncology clinical research trials.
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The Clinical Research Billing (CRB) Analyst plays a crucial role in overseeing the financial aspects of clinical trials within our highly regulated field. Certified Research Administrator (CRA), Certified Pre-Award Research Administrator (CPRA), Certified financial Research Administrator (CFRA), Clinical Research Contract Professional (CRCP), Certified in Healthcare Research Compliance (CHRC), Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), or ACRP Certified Professional (ACRP-CP.
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The Clinical Research Manager will work under the direction of the Institute Director and Institute Managing Director and with other institute leaders to plan the activities of the institute, be responsible for a broad range of duties related to planning, organizing, executing, and monitoring the implementation of new and existing clinical trials and research initiatives, and oversee clinical trial activities.
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Lead clinical research team through organization, preparation, and ongoing management of clinical trials. Experience in human-subjects research / clinical trials.
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Eligibility to serve as Principal Investigator for Clinical Trials in US. This position may be a good fit for a physician who has an interest in early phase clinical trials.
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The CRA will be responsible for monitoring and overseeing clinical trials to ensure compliance with regulatory requirements, Good Clinical Practice (GCP) guidelines, and study protocols.
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clinical trials jobs Title: research in New York, NY
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