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Job Overview-Robert Wood Johnson is seeking an Advanced Practice Provider to join the Cancer Center,This is a full-time opportunity to join a dynamic team at the state s only NCI designated Cancer Center,The ideal candidate is a self-motivated learner and able to collaborate with medical and nursing colleagues.
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New Jersey Urology is seeking a Patient Registrar to join our team in East Brunswick, NJ. This is an exciting opportunity for a dedicated professional who exudes compassion and care, and is dedicated to improving patient outcomes.
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Robert Wood Johnson is seeking an Advanced Practice Provider to join the Cancer Center,This is a full-time opportunity to join a dynamic team at the state s only NCI designated Cancer Center,The ideal candidate is a self-motivated learner and able to collaborate with medical and nursing colleagues.
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RWJBarnabas Health, the most comprehensive health care delivery system in New Jersey, is seeking a board certified physician in hematology/oncology to join our robust and well-established practice sites located in Central NJ. This unique position offers an opportunity to work closely with The Rutgers Cancer Institute of New Jersey, the states only NCI designated cancer center which offers access to ground breaking clinical trials, system wide tumor boards, and much more.
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The employee will be responsible for designing, conducting, and analyzing results of molecular cloning, gene expression analyses, cell culture work, tumor xenograft and allograft in mice, and genetically engineered mouse models.
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Job Summary: The Advanced Practice Nurse will care for inpatient solid tumor oncology patients. Job Summary: The Advanced Practice Nurse will care for inpatient solid tumor oncology patients. Exciting opportunity for Nurse Practitioner to join established Oncology/Hematology practice.
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RWJBH is seeking a Registrar for our Cancer Center at the New Brunswick campus. Oncology Data Specialist (ODS) by the National Cancer Registrars Association is required with working knowledge of medical terminology, anatomy, physiology, oncology disease process, coding, and staging.
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And other clinical trial activities for solid tumor, high enrollment, adult population Oncology related trials. 2 or more years of experience in clinical research as a Clinical Research Coordinator, with experience in patient recruiting/pre-screening/consenting/retention; activation; regulatory compliance, data management, and ensuring Serious Adverse Events (SAEs) are completed and reported within reporting deadlines outlined in the protocol.
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