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The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs. Join us as we continue to grow, the Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes & procedures, and in compliance with FDA, GCP, and ICH regulations and guidelines.
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Successful completion of GCP certification and Certified Clinical Research Coordinator (CCRC) certification preferred. High School Graduate and/or technical degree and 8+ years as a Clinical Research Coordinator.
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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 of Clinical Research Associates (SOCRA.
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The Clinical Research Manager (CRM) reports to, and is directly responsible to, the Assistant Director for the Clinical Trials Unit for all clinical research matters fulfilling the mission of the Chao Family Comprehensive Cancer Center (CFCCC), the University of California Irvine School of Medicine and the overall UC Irvine Health enterprise.
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This position will provide clinical research coordinator services on-site at Enloe Health Regional Cancer Center. The Clinical Research Coordinator (CRC) supports the clinical research efforts of the Cancer Care Network by providing comprehensive coordination and data management of complicated Phase I-IV cancer protocols according to Good Clinical Practices (GCP), internal standard operating procedure (SOPs), and University policies and procedures.
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The Clinical Research Coordinator (CRC) will oversee the execution of research studies according to established study protocols. The CRC will have direct contact with research participants, manage multiple clinical research projects/trials, and serve as a backup to other clinical research coordinators within the team.
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Cancer center in the Northern, NJ area is seeking an Oncology Clinical Research Coordinator. Certified Clinical Research Professional or Certified Clinical Research Associate or Certified Clinical Research Coordinator.
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Must have a minimum of a Bachelor’s degree in a health or science related field; Advanced degrees or prior clinical research experience is a plus; In-House CRA position available for those with no or minimal clinical research experience with rapid advancement.
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Certifications, licenses, or degrees as determined by the needs of the research projects, such as, registered nurse, nurse practitioner, certified mental health therapist/specialist, MSW, pharmacist, physical therapist, certified health education specialist, clinical psychologist, acupuncturist.
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Assist Director of Operations and Clinical Research Project Manager with supervision of at least one Clinical Research Coordinator I/II. Under the direction of the Director of Operations and Clinical Research Project Manager, the Clinical Research Coordinator will work independently on ongoing research studies.
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The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them.
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Clinical Research Coordinator, Norwalk, CT. Reports to Director of Clinical Trials or Clinical Research Nurse Lead: Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies.
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JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: The Clinical Veterinarian is responsible for a wide spectrum of duties including professional veterinary and administrative services in laboratory animal medicine, biomedical research support, and education.
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Participates in internal study start-up processes with Office of Grants and Sponsored Programs and works collaboratively with the Clinical Research Associate/Assistant and internal Regulatory Study Start-up Specialist to complete all regulatory documents.
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The Clinical Research Coordinator (CRC) will independently, or with general direction, execute, manage, and coordinate clinical research protocols, as directed by the Clinical Research Manager, Principal Investigator (PI), and/or the Research Personnel Director for the Breast Oncology program.
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clinical research jobs Title: instructor Company: University Of Colorado
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