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Christiana Care Health System is currently seeking a Research Nurse Coordinator with two years of Oncology Clinical experience for our Cancer Research Department at the Helen F. Graham Center & Research Institute in Newark, DE.
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At each of our 12 multidisciplinary disease site centers, patients have a fully dedicated team that include oncologists, surgeons, navigators, and social workers, as well as a clinical research nurse at each MDC to explore avenues for potential cutting-edge treatments in the latest clinical trials.
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Serves as a preceptor and mentor for new or less experienced research nurse coordinators, clinical research associates, and support staff. Follows study-specific protocol guidelines, communicates, and interacts with investigators, hospital staff, department manager, sponsoring agencies, and others to effectively perform clinical research activities.
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The department of Computational Biology is seeking an experienced Bioinformatics Research Scientist to lead the development of bulk and single-cell RNseq-based pipelines for use in our clinical genomics program.
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In this role the Research Nurse Coordinator screens, enrolls, plans, implements, and evaluates protocol-related care of participants and data for assigned research projects. Research Nurse Coordinator (RN.
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Job Introduction: As a Clinical Research Coordinator, you will execute and coordinate a variety of specialized clinical research activities within the Early Phase Clinical Unit (EPCU), ensuring that assigned protocols are executed with high quality, and Standard Operating Procedures (SOPs)and GCP/ICH guidelines are followed.
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Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country.
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Responsibilities: Conducting all trial visits Completing all study-specific assessments (e.g. vital signs, EKG, blood collection) Processing all samples and shipping to Central Lab Maintaining study source Entering data into sponsor EDC and query resolution as the sole Senior Clinical Research Coordinator (SCRC) on-site, the chosen candidate must be adept at protocol comprehension and be capable of working autonomously.
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Job Description: The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials.
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We’re bringing together top talent from academia, industry, and startups to build a new model for innovative R&D. As an incubator within the Schmidt Futures Network, we identify high-impact scientific or technical research and development opportunities, ultimately defining and launching these projects as Focused Research Organizations.
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Job Summary The Clinical Research Coordinator will support the research programs of Dr. Garber, including multi-site, NIH-funded studies of refeeding in body composition in anorexia nervosa, and a new pilot study on microbiome recovery in malnutrition.
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The Cell Therapy Attribute Sciences department is seeking a Senior Research Associate to support the development of gene-engineered T-cell products. The primary focus of the Senior Research Associate – Attributes role will be to build CAR/TCR T cell product and process understanding in support of early and late-stage CAR T with a particular focus on exploratory/investigational needs for mid-stage programs.
$52.45 an hourExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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We are seeking a Clinical Research Coordinator I to support the Naval Health Research Center (NHRC), Operational Infectious Diseases (OID) Directorate by coordinating and managing clinical research studies.
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The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, communicating non-medical trial concepts and details, and participating in the informed consent process.
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Job Code: 00000803 CLINICAL RESEARCH SPECIALIST, SR. Know and follow policies, standard operating procedures (SOPs), regulations and protocol requirements that govern clinical research.
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clinical research jobs Title: coordinator regulatory Company: Boston Medical Center Bmc
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