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The Clinical Research Coordinator A will also be responsible for training new personnel who will be working on clinical trials within the division. The Clinical Research Coordinator A will recruit and screen patients as outlined in research protocols, will coordinate all research visit activities for assigned projects (including processing and shipping blood and urine samples), and will assist in the maintenance of research records in compliance with IRB and HIPAA regulations.
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Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC.
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Clinical Research Coordinator ( 2 positions) School of Medicine, Internal Medicine/Pauley Heart CenterVirginia Commonwealth University (VCU) School of Medicine is a premier academic medical center located in the heart of Richmond.
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The Clinical Research Coordinator 2 works under the general direction of the Director of Clinical Research and a Senior Clinical Research Coordinator within the Pediatric Clinical Trials Office, as well as the study PI team.
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Our research aims to improve quality of life, well-being, symptom and pain management, and reduce caregiver burden:For example, a Clinical Research Coordinator to support a large multi-site clinical trial study that focuses on the comparison of care delivery models to support older adults with complex healthcare needs.
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Sentara Heart Hospital located on the campus of Sentara Norfolk General Hospital is hiring a Cardiovascular Research Nurse to support the Clinical Trials Office! Specialty certification Certified Clinical Research Professional (SOCRA CCRP or ACRP-CP) or Certified Clinical Research Coordinator (CCRC) is required within 3 years of employment.
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The Clinical Research Coordinator (CRC) works with the CommonSpirit Health Research Institute Research Operations Market Research Manager (MRM), Principal Investigators, co- and sub-investigators, Senior Clinical Research Coordinator, clinical and ancillary departments, IRBs, and industry or government sponsors of research to support the planning, implementation and coordination of clinical trials and other research projects managed by the CommonSpirit Health Research Institute.
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Minimum 3 years of experience conducting clinical trials required; worked as primary research coordinator for at least 5 drug or device trials. Under the direction of the MRM and/or Senior Clinical Research Coordinator, the incumbent helps to ensure compliance of the research program and its studies with all applicable federal and state regulations, as well as CommonSpirit Health policy.
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It has direct responsibility for implementing a diverse portfolio of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities, such as a clinical database and biorepository.
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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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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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The Clinical Research Coordinator performs study coordination tasks under the direction of the investigator and works closely with the Senior Research Scientist to ensure overall compliance in the conduct of the study, and adherence to the approved study protocol.
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Job Description: The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials.
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Responsibilities: Conducting all trial visits Completing all study-specific assessments (e.g. vital signs, EKG, blood collection) Processing all samples and shipping to Central Lab Maintaining study source Entering data into sponsor EDC and query resolution as the sole Senior Clinical Research Coordinator (SCRC) on-site, the chosen candidate must be adept at protocol comprehension and be capable of working autonomously.
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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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clinical trials research coordinator jobs Company: Perelman School Of Medicine University Of Pennsylvania
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