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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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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.
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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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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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Must have proper experience and demonstrate mastery of Clinical Research Coordinator I position. Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
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Bachelors degree from a recognized college or university in a science or health-related field, or six (6) years of clinical research, healthcare or related field in lieu of degree. Develops and maintains basic competencies required to conduct clinical research including maintaining current training records.
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Knowledge, Skills and Abilities: Thorough understanding of the clinical research process (i.e., GCP, SOPs, informed consent, safety monitoring, etc.) Conducts clinical studies according to FDA/GCP and ICH regulations and guidelines.
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