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One or more years of clinical research experience Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred. ADDITIONAL JOB RESPONSIBILITIES:The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials and mixed methods research specific to LGBTQ+ populations.
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Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional. If not Certified Clinical Research Coordinator (CCRC) or a Certified Clinical Research.
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Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional(CCRP) through the Association of Clinical Research Professionals (ACRP) or the Society ofClinical Research Associates (SOCRA.
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No previous experience in clinical research years of required, but must have general medica lpractitioner diagnosis and treatment proficiency. Conducts all clinical trials (studies) according to ICH GCP, local regulations, study protocol and company processes.
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The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials and mixed methods research specific to LGBTQ+ populations.
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As a Clinical Research Coordinator, you will be planning, coordinating, evaluating, and performing care of participants while collecting data for assigned research projects. Job Title: Clinical Research Coordinator II.
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Join our team as a Remote Clinical Research Associate III to contribute your expertise in site management and field monitoring towards impactful clinical trials. Experienced Remote Clinical Research Associate III Opportunity.
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Completes research administrative duties according to Children’s policies regarding Epic enrollment, Clinical Trial Management System data entry, patient care invoice accuracy. Assist with facilitating grants, contracts, and financial tasks for research and clinical trials.
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Develops and maintains basic competencies required to conduct clinical research including. One year of experience in clinical research, healthcare, or related field. Responsible for coordinating clinical research projects.
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Certification by an industry-recognized professional society (i.e. Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP) or accredited institution.
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Whether you are healthy, or have a specific illness, we'll connect you with the right trial.
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Or master's degree, MD or PhD in a scientific, health related, or business administration program and two years of clinical research experience Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred.
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The Clinical Research Coordinator will also be supporting the research manager in training research assistants and corresponding with sponsors and IRB’s. The Clinical Research Coordinator is responsible for supporting the needs of the clinical research department and the Investigators.
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Research Project: Joining the Clinical Research, Epidemiology, and Outreach (CREO) team at CVDB, the selected participant will provide epidemiological and statistical and/or data application support for the research in ME/CFS or Long COVID ME/CFS-like illness.
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A minimum of 2 years of on-site monitoring experience is required, however monitoring experience may be waived if relevant Novo Nordisk experience is demonstrated in GCP-related clinical research.
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Title: clinical research in Atlanta, Schuyler, Nebraska
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