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As an official table tennis sponsor for three Summer Olympic Games and the official sponsor of pickleball's top athletes and the Professional Pickleball Association (PPA), the team at JOOLA combines its storied expertise with fresh perspectives to bring innovation to both sports.
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Communicate effectively with subjects, research team, Institutional Review Board (IRB) and sponsor representatives. Clarify questions and concerns with the investigator and sponsor regarding enrollment goals, sponsor expectations and study procedures.
$27.5 - $44 an hourFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The Clinical Research Coordinator A (CRC)will be responsible for patient screening, subject enrollment, scheduling, collection, storage and shipment of biological samples; collection and filing of study documents; and collection and entry of clinical data.
$37,220 - $52,661 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Business Segments Include:Corporate & Institutional MarketsCorporate and Institutional Markets group includes loan syndications, leveraged finance, fixed income and equity capital markets, financial sponsor coverage as well as mergers and acquisitions, and private/alternative capital advisory for middle market companies.
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Demonstrated experience or knowledge with sponsor or CRO clinical research process, including collection of documents at study start-up, during study conduct and close-out. This position is responsible for collecting, reviewing, maintaining, and archiving essential Regulatory documents for the Trial Master File (TMF) in accordance with Good Clinical Practice (GCP), E6 ICH Guidelines and other regulatory guidance documents, relevant regulations (e.g., 21 CFR Parts 312 and 314, EMA Clinical Trials Directives), and Arcus Standard Operating Procedures (SOPs) as appropriate.
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THE Clinical Research Associate (CRA) Role The CRA is an important member of the Alira Health Clinical team. Clinical Research Associate page is loaded Clinical Research Associate Apply locations Boston-Remote time type Full time posted on Posted 2 Days Ago job requisition id JR000112 Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration.
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Participate in 133 federal research and other sponsor audits: Ensure that all federal grant documentation and ledger accounts are in order for examination by external auditors. The Director works collaboratively with faculty, foundation and corporate philanthropy, advancement, corporate partnerships, Institute, and The Claremont Colleges Services business offices to foster a robust sponsored project pipeline and ensure compliance with all federal and sponsor regulations and donor designations related to extramural funding.
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Overall, the CRC is the site's primary liaison among research participants, the local investigator(s) and study sponsor(s). The Clinical Research Coordinator (CRC) is a specialized, independent research professional who ensures oversight and compliance of both system-wide and local SHC clinical research activities.
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OSP works with campus research faculty to prepare budgets, ensure compliance with UC Policy and sponsor guidelines, and signs on the final submission. 10% - Pre-Award Consultation Provides guidance and counsel on pre-award research administration matters to departmental/divisional/central office grants administrators related to terms and conditions, pertinent Federal/State regulations, sponsor requirements, and UC Policy in contract and grant management.
$78,000 - $84,000 a yearExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The director will develop new business growth opportunities for the MITRE Accelerator focused on sponsor impact and collaboration with private sector organizations. Conduct market research to identify emerging trends, competitive landscapes, and potential opportunities for the MITRE Accelerator.
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JOB SUMMARY: The Senior Fellow is expected to lead initiatives, conduct, publish, and promote in-depth, high quality public policy research and learnings, convene public events engage with a wide range of stakeholders, Project Management, and work on policy and practice relevant publications intended to advance the field of equitable community development.
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The Clinical Research Associate/Clinical Research Coordinator I (CRA/CRC I) works under general supervision to enroll eligible patients to clinical research protocols and manage all aspects of data collection and submission for multiple cancer studies.
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As the primary resource for the protocol, the Clinical Research Coordinator III acts as a liaison between the patient, investigator, Institutional Review Board, and sponsor. Certification as a Certified Clinical Research Coordinator (CCRC through the Association of Clinical Research Professionals or ACRP.
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Ensures compliance with all appropriate NU policies & practices; local, state, federal, agency & sponsor rules, regulations & requirements regarding grant &/or contract administration. SCS course: Grantsmanship for the Research Professional.
$67,978 - $95,595 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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The SOM CTO provides budget and billing support to clinical research teams such as clinical trial budget development, study billing coverage analysis development, Epic billing reconciliation, and sponsor invoicing.
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