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Oversee all EDC,and IRT vendor contracts for assigned clinical trials. Manage and maintain vendor budgets for assigned clinical trials and process flows and data exchanges with global pharmacovigilance for clinical trial serious adverse events.
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The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.
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Responsibilities Process and perform quality control of expedited and non-expedited Serious Adverse Event (SAE), Adverse Events of Special Interest (AESIs), Pregnancy, Aggregate and Signal Detection Reports for all DAIT clinical trials for consistency, reportability, completeness and accuracy.
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What Makes You Awesome: Registered Nurse RN license in the state of Florida or ability to obtain Certified Clinical Research Coordinator CCRC ACRP Progressive background in oncology research and clinical trials This established organization is located in one of southern Florida’s most popular coastal metropolitan areas.
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Previous experience working in a matrixed environment to implement flow cytometry assay development and validation to support clinical trials. In this vital role you will design, develop and implement clinical biomarker assays employing innovative flow cytometry methods and techniques to support our drug development efforts.
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We are recognized by the American Society of Clinical Oncology (ASCO) with a national Clinical Trials Participation Award, FCS offers patients access to more clinical trials than any private oncology practice in Florida.
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This one-year fellowship opportunity is for physicians to be mentored in the translational neuroscience program headed by Elizabeth Berry-Kravis, MD, PhD. As the leading investigator in multiple NIH-funded research programs and industry-and foundation-sponsored clinical trials, Dr. Berry-Kravis has established Rush University Medical Center as an international destination for rare disease treatment and research in the area of pediatric neurodevelopmental and neurogenetic conditions.
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Experience drafting and negotiating clinical trial agreements. Experience with clinical trial and/or research agreements with ability to handle increasing levels of responsibility. Support strategic initiatives of the VP/ Deputy General Counsel and EVP/ General Counsel.
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Implement a modeling & simulation strategy to assist and accelerate decisions around preclinical study design and interpretation, as well as prediction of first-in-human dose and safety margins for clinical trials.
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The Clinical Research Supervisor reports to the Research Administrator, Clinical Trials Manager, Research Vice Chairs and works directly with Principal Investigators within the Department of Obstetrics, Gynecology and Women's Health on the execution of reproductive health research studies, focusing on protocol development and coordination, supervising research/study assistants, and data cleaning and monitoring.
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Overview The CTO PI-Initiated Research Project Manager (CTO RPM) for Waldenstrom’s Macoglobulinemia Think Tank Network (WM-NET) is responsible for assigned day-to-day coordination and overall management of WM-NET activities for assigned clinical trials and program; primarily multi-center, PI-initiated trials.
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Prior experience in providing MSL-level support to products or devices in endocrinology and/or rare disease, including KOL development, investigator-initiated clinical trials, publications and educational programs, highly preferred.
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At Cedars-Sinai Cancer, we offer state-of-the-art treatments, experimental therapies, next-generation research, and cutting-edge clinical trials for over sixty types of cancer at more than ten locations throughout Greater Los Angeles.
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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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As a Quantitative Systems Pharmacology Modeler - Senior Scientist in DMPK & Modeling, you will be empowered to interface between clinical pharmacology, clinical research, nonclinical drug safety, drug discovery, drug metabolism, translational medicine and pharmacovigilance to influence drug development.
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clinical trials jobs Title: analyst Company: Integrated Resources Inc Iri in Parkville, Maryland
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