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Bachelor degree from an accredited college or university in chemistry, biology, biochemistry, cell biology or other natural, life, health care or materials science directly related to the research area to which the position is assigned and experience in a research, basic science or clinical setting particularly clinical trials research.
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The research portfolio of the Dermatology Service includes optical engineering, artificial intelligence, basic science, translational science, epidemiology and clinical trials with over $5 million of annual funding from NIH, Foundations, Industry, and philanthropic sources.
$150,000 - $510,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Candidates for this position should have a strong academic track record and be prepared to build a strong research enterprise in areas such as clinical trials, quality improvement, translational medicine, precision medicine and population health.
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Education and/or experience Bachelor’s degree, preferably in areas such as biological sciences, health care management or life sciences research; BSN/RN or experience with management of clinical trials.
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In 2009 and 2013 our practice received the ASCO clinical trials participation award. We have been members of the Jefferson Cancer Network since its inception and received JCN clinical trials awards.
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Contribute to the identification of new sites for clinical trials; analyse capability and support CRMA and CSM in making recommendation for trial inclusion. ICON plc is a world-leading healthcare intelligence and clinical research organization.
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We participate in clinical trials and are funded in areas ranging from asthma, allergic rhinitis, food allergy, hereditary angioedema and primary immunodeficiency. The Division of Allergy and Clinical Immunology evaluates and treats both children and adults at our primary Milwaukee site, located in the Children’s Wisconsin Craig Yabuki Tower, and at all our “Care Closer to Home” sites around the area.
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The Clinical Research Coordinator (CRC) is central to conducting and managing clinical trials, tasked with obtaining informed consent, executing study protocols, handling human specimens, and ensuring meticulous documentation and communication.
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UPMC Hillman Cancer Center is currently hiring a regular full-time Clinical Research Nurse Coordinator (RN) to help support the Community Oncology Clinical Research Services (CRS) teams at Beaver and Moon/Sewickley located in Beaver, PA & Moon/Sewickley, PA. This position offers a $6,000 sign-on bonus and will work a regular Monday through Friday daylight schedule with the Beaver (primary site) & Moon/Sewickley Medical Oncology network locations but may go to other sites in the area as needed.
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S/he will partner closely with Dr. Garber, work with her project managers to provide support to their projects, but will particularly focus on developing and implementing prevention trials, working most closely with the prevention team at Dana-Farber and leading the development of clinical trials as part of collaborations with external sites, locally, nationally and internationally.
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Provide clinical physics support to our central Ohio Radiation Oncology care sites, including daily operations, routine quality assurance activities, support for SBRT treatments, support for SRS treatments, intravascular brachytherapy, HDR, chart checks, support department adherence to policies and procedures, and support all aspects of participation in clinical trials.
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Extensive multidisciplinary support including site-specific tumor boards at Virginia Mason and St. Francis Hospital Involvement in collaborative group clinical trials. At Virginia Mason Franciscan Health you will find the safest and highest quality of care provided by our expert, compassionate medical care team at 11 hospitals and nearly 300 sites throughout the greater Puget Sound region.
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Their sites conduct Phase I-IV trials in therapeutic areas like cardiology, metabolic disorders, renal, CNS, pulmonology, women's health, and vaccines. Our client is a Clinical Research site network with over 17 research sites across the United States.
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Collaborate with sites participating in clinical trials in preparing regulatory documents for submission to central IRB's for approval. Distribute clinical trial protocols and feasibility questionnaires to investigators interested in participating in trials as appropriate.
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Our department is responsible for developing vaccine adjuvants and drug products from preclinical studies through Phase III clinical trials with line of sight to commercialization. Primary responsibilities of the role include design, execution, and documentation of experiments to develop stable formulations and robust manufacturing processes for preclinical and clinical supply production and to scale-up these processes to the pilot plant and commercial space.
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