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Our core practice areas include: clinical research; vaccine research, microbiology and infectious disease research, development and production; biodefense; global health security; and HIV/AIDS programs.
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Tracks site budget and investigator grant estimates when needed via Medidata Grants Manager. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma.
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The Staff Scientist I is a junior career research position that reports to the principal investigator. Conducts research and development of new next generation sequencing clinical assays.
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Current certification in health care fraud investigation, such as Accredited Healthcare Fraud Investigator (AHFI), Certification as an Internal Auditor (CIA), Healthcare Compliance certification (CHC), or equivalent.
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Design high quality & innovative clinical trial protocols (including all supporting documents such as Investigator s Brochure, informed consent, etc) for lead Oncology target programs that are aligned with the Clinical Development Plan and overall product strategy.
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Required and Current certification as NP. required and Current certification in BCLS. required andCDE - Certified Diabetes Educator Certification Certified Diabetes Educator or CDE eligible preferredKnowledge, Skills, and AbilitiesRecognized clinical competency with sensitivity to the psychological, social and medical needs of patients.
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Date Posted Friday, January 12, 2024 Position is with Lab/Branch/Program Name of Hiring Official/Investigator Job Description A postdoctoral position is available in the lab of Dr. Stavroula Mili in the Laboratory of Cellular and Molecular Biology, National Cancer Institute, NIH, Bethesda, MD.Dr. Mili's research program focuses on the roles of localized mRNAs in mammalian physiology and tumor progression.
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Assist in the gathering of EDC design requirements from stakeholders and to address the needs of sites (e.g., investigator, study coordinator, study monitor). Working knowledge of Clinical database applications such as EDC and CTMS. Knowledge of general medical coding in the pharmaceutical/biotechnology industry including knowledge of medical dictionaries, coding tools, and coding governance models.
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Gather and analyze data resulting from the collaborative research to be used for identifying disease protein profiles and biochemical and metabolic changes to complete the clinical characterization, as well as metagenomics/ microbiome sequencing.
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The Research Assistant will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations and Food and Drug Administration (FDA) regulations.
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Access to NIH's unparalleled resources and niche scientific initiatives OBJECTIVE: Support the Principal Investigator of ANPL with laboratory organization, administrative tasks, and assuring adherence NIH guidelines and policies for clinical research.
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We are currently searching for Administrative Laboratory Manager to provide support to the Principal Investigator of ANPL with laboratory organization, administrative tasks, and assuring adherence NIH guidelines and policies for clinical research.
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Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company or as a principal investigator (comparable to 1-2 years) in the industry; Or. Working knowledge of biostatistics, data management, and clinical operations procedures.
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Provides medical review and analysis for clinical trial serious adverse events, marketed products ICSR and periodic safety reports ( e.g. PBRER, PSUR, DSUR) as well as other client deliverables (e.g. labeling reconciliation documents, CTD modules, REMS, RMP and CSR.
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The Clinical Research Assistant performs a variety of research, data and clerical duties of a routine and technical nature to support the conduct of clinical research under the direction of a senior research team member.
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clinical investigator jobs in Chevy Chase, MD
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