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Clinical Research Coordinator II - Onsite Onsite in Tustin Ca. and Redlands Ca. Why work at Tilda? As a Clinical Research Coordinator II with us, you will play a vital role in the advancement of medical science and the development of groundbreaking treatments.
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The Clinical Research Coordinator (CRC) is an integral and essential member of the ACC CRU Developmental Therapeutics Research Team. We are looking for an enthusiastic, professional and committed team member to work closely with our clinical research investigators, Research Team Leaders, our clinical research nurse(s), and regulatory coordinator.
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High School Graduate and/or technical degree and 6 years as a Clinical Research Coordinator/Clinical Research Associate. Bachelor’s degree and minimum of 2 years’ experience as a Clinical Research Coordinator/Clinical Research Associate OR.
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Job Description: GDIT's Military Health Team is seeking an Assistant Clinical Research Coordinator in support of the Naval Health Research Center (NHRC) Operational Infectious Disease (OID) Field Surveillance and Laboratory Research Services.
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The clinical research coordinator (CRC) will be trained to conduct human neuroimaging research with a number of tools, including administration of TMS inside and outside of an MRI scanner.
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Under the direction of the Principal Investigator (PI) and Cardiology Research Nurse Manager, collaborate with all members of the clinical research team to ensure all federal, state, university, and protocol requirements are followed, institutional research objectives are met, and that ethical obligations are kept.
$55,000 - $75,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Education, Knowledge, Skills and Abilities Preferred: BSN PreferredMandatory education on human subject research and GCP (CITI Training and Certification)Knowledge of clinical trials and the regulation (local, state, and federal) of suchFamiliarity with basic scientific and healthcare principles and terminologyAbility to work in a fast-paced environment and manage competing tasks and demandsLicenses and Certifications Required:NJ State Professional Registered Nurse License.
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Job Req ID: 112971 Clinical Research Monitor The Department of Neurology is seeking a who will take the lead on compliance monitoring of predominantly large, multi-centered, clinical trials in keeping with established BIOS Clinical Trials Coordinating Center (CTCC) policies and procedures and GCP. The CRM will ensure quality, accuracy and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials through utilization of a risk-based, remote monitoring approach.
$55,200 - $96,600 a year depends on experienceFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Odyssey is seeking a Registered Nurse (RN) for a Clinical Research Nurse Coordinator position to support the Clinical Investigation Department (CID) in the Cancer Coordination Center at the Navy Medical Center, Portsmouth (NMCP) Virginia.
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Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA) Certified Research Associate (CRA), Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), or comparable.
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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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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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Preferred: Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) is preferred. Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) certification, along with a minimum of two years additional professional experience, will be considered in place of degree.
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The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study.
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This includes frozen sections, special stains, immunohistochemistry and electron microscopy for both clinical and research neuromuscular samples. Responsibilities Performs research and clinical diagnostic histology and electron microscopy experiments independently or semi-independently in accordance with protocols approved by the principal investigator.
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clinical research jobs Title: registered nurse Company: Davita
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