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POSITION SUMMARY:The Clinical Research Associate II (CRA II) will be a key contributor to AtriCure’s clinical affairs department and primarily responsible for the site management of assigned clinical investigative CRA II will assist with the implementation and execution of study protocols and associated study documents for clinical trials, including clinical monitoring of AtriCure also includes the coordination of site activities from site start-up to site closure as needed.
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Clinical Research Associate II Cincinnati, OH, USA ● Mason, OH, USA ● Minneapolis, MN, USA ● Minnetonka, MN, USA Req #1992 Friday, March 22, 2024 AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions.
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Clinical research, Oncology, inpatient, Gcp, Irb, Data management, BLS, CPR, AED, Registered Nurse, communication and leadership skills, CCRC or CCRP Certified, patient registration, quality assurance, subject eligibility, EMR, clinical trial, regulatory, oncology nursing, chart review, enrollment, adverse event reporting.
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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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Research associate, RA, infectious disease, flu, influenza, life sciences, preclinical, cro, contract research organization, in vivo, research, research study, animal studies, mammalian cell, bsl 2, glp, sop, sops, standard operating procedures, lab, laboratory, vaccine, research and development, elisa, immunology, immunoassay, pipetting, centrifugation.
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Under the supervision of the CNS East Asia Program Director, the Research Associate will assist in the operations and implementation of activities tasked to and performed at CNS, as described in the duties below.
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See job description Heluna Health invites applications for a Research Associate position in the Center for Public Health Research (CPHR) at the San Francisco Department of Public Health.
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Certification as a Clinical Research Associate or Coordinator. Reporting directly to the Disease Team Project Manager, the Clinical Research Coordinator I is responsible for coordinating and managing clinical trials including providing all aspects of protocol management, including screening for patient eligibility, data collection and analysis, ensuring protocol compliance, adverse drug reaction reports, monitoring patient treatment and toxicities, laboratory and specimen submission, and maintenance of accurate and complete clinical research files.
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Certified Clinical Research Associate (CCRA) credentialing. 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 2 days ago - UpvoteDownvoteShare Job
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Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, is one of the world's leading oncology research organizations conducting community-based clinical trials. In 2022, SCRI formed a joint venture with former US Oncology Research to enhance clinical trial access and availability across the country.
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Our primary offerings include: Program Design and Strategy DevelopmentProgrammatic Research, Analysis, and ModelingGrant Support: Sourcing, Conducting Due Diligence, Making Grant Recommendations, Grantee ManagementProject Incubation, Nonprofit Business Planning, Organizational Development, and Staffing SupportEvaluation and LearningFacilitation, Collaboration, and Grantee ConveningRecruiting and Organization Design About the RoleCEA is looking for a Research Associate.
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Other areas of interest include outcomes research and health equity research. Other areas of interest include outcomes research or health services research. Educator to convey principles of research development, grant writing, publishing/disseminatingExperience in collaborating with communities and stake holdersCommitment to evaluating inter-departmental collaborations.
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The Physics Department has an opening for a research associate in the Nuclear Theory Group. BNL policy requires that after obtaining a PhD, eligible candidates for research associate appointments may not exceed a combined total of 5 years of relevant work experience as a post-doc and/or in an R&D position, excluding time associated with family planning, military service, illness or other life-changing events.
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Clinical Research Coordinator II Full-time, 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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Job DescriptionTexas A&M AgriLife Research Center at Beaumont, TX is seeking a postdoctoral research associate who possesses a strong background in plant pathology with experience in both fundamental and applied research.
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Title: clinical research associate Company: Ppd
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