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Our work ranges from basic to translational and clinical, and our clinical trials are conducted in the NIH Clinical Center, the world’s largest hospital dedicated to clinical research that offers a robust infrastructure to support CCR’s patients on an estimated 250 open studies.
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The Research Data Coordinator 2 is responsible for data management for phase I, II, and III oncology clinical trials conducted in the Lombardi Comprehensive Cancer Center (LCCC). + Support all aspects of clinical research data management for clinical trials conducted in the LCCC Clinical Research Management Office (CRMO), including collection of data from source documents and medical records and completion of case report forms per sponsor requirements.
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Act as a clinical research pharmacist consultant by collaborating with domestic and international clinical research networks to develop and implement clinical trials, direct start-up activities, coordinate clinical site preparation/renovation, assess factors that may significantly affect a site’s clinical research and pharmacy capacity/operations, and devise solutions and/or approaches to mitigate potential issues.
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The qualified candidate will report to the Head of Clinical Data Science and is expected to have the following responsibilities:· Perform integrative analyses of multi-omics data from clinical trials and research cohorts, including genomics, transcriptomics, proteomics, and imaging, to identify biomarkers related to treatment mechanism and response, and potential therapeutic targets.
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We are examining therapeutic targets for traumatic brain injury (TBI) and evaluating candidate therapeutics for repurposing to TBI as a new clinical indication. The person selected for this position will conduct research in experimental models to screen therapies to promote regeneration and plasticity to protect against neurodegeneration and chronic symptoms associated with traumatic brain injury (TBI) and related clinical conditions.
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Certification(s): Certified Cryptocurrency Investigator - Blockchain Intelligence Group (CCI)" (U) Certification(s): Certified Cryptocurrency Investigator - Blockchain Intelligence Group (CCI.
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NCH is transforming into an Advanced Community Healthcare System(TM) and we’re proud to: Provide higher acuity care and Centers of Excellence; Offer Graduate Medical Education and fellowships; Have endowed chairs; Conduct research and participate in national clinical trials; and partner with other health market leaders, like Hospital for Special Surgery, Encompass, and ProScan.
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Professional Certified Investigator (PCI) - ASIS International. The Office of Military Commissions (OMC) and Military Commissions Defense Organization (MCDO) require an investigator to support defense counsel in multiple areas of pre-trial investigation and trial preparation for the Military Commissions convened under the Military Commissions Act of 2009.
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The Staff Scientist III position is a senior role requiring a PhD degree and reporting to a principal investigator or CNRI center director. The Staff Scientist III supervises junior scientists, graduate students and technicians and works independently or with technical guidance from the principal investigator.
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Develop novel methodologies for analyzing immunological and pharmacokinetic data from both vaccine and monoclonal antibody clinical trials. Responsibilities Provide accountability for the scientific deliverables and contributions of the Vaccine Research Center’s (VRC) Translational Science Team. Oversee essential team functions, ensuring that: All scientific objectives of VRC clinical trials are met; Clinical trial data is accurately analyzed and project timelines established by VRC leadership are met.
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Accredited Healthcare Fraud Investigator (AHFI) Certification, Health Care Anti-Fraud Associate (HCAFA) Certification, Certified Insurance Fraud Investigator (CIFI) Certification, Certified in Healthcare Compliance (CHC) Certification, Certified Fraud Examiner (CFE) Certification or Certified Financial Crimes Investigator (CFCI) Certification.
$73,100 - $166,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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As a Surveillance Investigator at Ethos Risk Services, you will conduct covert surveillance, review files, and draft detailed case reports. What does aN Experienced FIELD Surveillance Investigator do.
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Conduct clinical research according to approved protocols as a study Principal Investigator, Protocol Chair, Associate Investigator, Consultant, or other designated role and maintain ethical and regulatory compliance as well as the integrity of study data and health and welfare of study participants.
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The purpose of the interview is to determine whether candidates possess the personal characteristics necessary to perform the duties of aviation safety investigator positions successfully. The National Transportation Safety Board (NTSB) offers a comprehensive benefits package that includes, in part, paid vacation, sick leave, holidays and various benefits as well as work life amenities such as alternate work schedules, telework, flextime, fitness and transit benefits.
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With 15+ years of experience in this space, our teams have supported 1000s of clinical trials, 100s of EDC builds for a multitude of Sponsors/CROs. With a long-standing alliance with Medidata (now Dassault Systems), the leading EDC platform solution provider, we have been successfully implementing Medidata’s best-of-the-breed products to help execute very complex mega-trials for our premium customers.
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clinical trials investigator jobs in Washington, DC
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