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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 #2009 Monday, April 1, 2024 AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions.
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POSITION SUMMARY:We are seeking a capable Jr. Clinical Research Associate (CRA) to be responsible for assisting the clinical team in planning, initiating, and monitoring Clinical trial sites as well as tracking enrollment and site engagement activities.
Full-timeExpandUpdated 21 days ago - UpvoteDownvoteShare Job
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We’re seeking an experienced Senior Clinical Research Associate to join the Veterinary Operations team that achieves its mission through developing veterinary partnerships, engaging with the veterinary community through education, ensuring excellence in the science behind our products, executing clinical trials and studies.
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Abiomed, part of Johnson & Johnson's MedTech, is recruiting for a Clinical Research Associate. Reporting to the Lead Clinical Research Associate, the person in this role is responsible for the management of day-to-day aspects of investigational site activities on assigned clinical trials.
$95,000 - $125,000 a yearFull-timeExpandUpdated 21 days ago - UpvoteDownvoteShare Job
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Have experience in clinical research and/or product development in animal health. Perform User Acceptance Tests (UAT) of the Electronic Data Capture (eDC) system and other clinical trial software.
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For CRA I: 1+ years direct clinical research experience at a sponsor, CRO, device manufacturer, IVD, companion diagnostics or investigator site. For CRA II: 3+ years direct clinical research experience at a sponsor, device manufacturer, IVD, companion diagnostics or CRO as a CRA/study monitor or equivalent experience.
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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.
$30 - $45 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Licenses and Certifications Preferred:Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC.
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Prepares for study visits: research bio-specimen collection order preparation/placement, laboratory and EKG order placement, scheduling of biopsies and scans, facilitating RECIST form completion from the investigator, AE and ConMed form completion in conjunction with a licensed professional (CRN/APP/MD) and other tasks as needed to support the administrative conduct of clinical trials.
$63,935.04 - $75,000 a yearFull-timeExpandUpdated 20 days ago - UpvoteDownvoteShare Job
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Train and shadow with various clinical research departments, including Dana-Farber Adult and Pediatric Clinical and Regulatory Teams, Dana-Farber Departments: Grants & Contracts, Office of Clinical Research (OCR), Dana-Farber/Harvard Cancer Center (DF/HCC) Offices: The Office of Data Quality (ODQ), and Office for Human Research Studies (OHRS.
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Certified Clinical Research Associate (CCRA) credentialing. The Department of Neurology is seeking a Clinical Research Monitor (CRM) 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.
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JOB OBJECTIVE: The clinical research scientist will provide pharmacology and pharmacogenetic support and execution of the development and update of the TRHC’s clinical decision support system (CDSS) on multi-drug-drug interactions based on drug pharmacokinetics and pharmacogenetic properties.
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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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PREFER: Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), or certified within 2 years. Function independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporations.
$27.91 - $51.83 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago
Title: clinical research associate Company: Thrive
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