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Maintains records in accordance with various regulatory agencies and enters patient and study information into the radiology information system, and documents billing codes of procedures performed to ensure accurate patient charges.
$2,832 a weekExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Nurse Coordinator will assist regulatory coordinators with communicating with the Institutional Review Board (IRB) and communicating treatment modifications and amendments, confirms appropriateness of drug doses in accordance with protocols, acts as a consultant to members of the health care team, and prepares and responds to audits conducted by study sponsors.
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Strong experience in patient centered outcomes research: COA instrument development/psychometric validation, quantitative analysis of CObased clinical study endpoints, regulatory dossier development and submissions.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Preferred Degree Preferred: Bachelor of Science Field of Study: Meat Science, Food Science or closely related field Experience. Participate as a team member in maintaining the meat processing activities and facilities in compliance with appropriate regulatory agency regulations, directives, guidelines, and policies and cooperate with [appropriate regulatory agency] regarding sanitation, operation and regulation of all meat processing areas.
$140,000 - $160,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Assist sites in central IRB on-boarding, ensure timely and accurate submission to IRBs, sponsors and master agreements, local IRB/ethics committee review/approvals, and assist with the collection of all necessary regulatory documents needed before site activation for study subject enrollment.
$54,080 - $94,710 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Monitors study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional policies. The Clinical Research Nurse, under general supervision, serves as the primary technical support to a clinical drug trial or other research study, the scope and complexity of which requires licensure as a Registered Nurse.
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For more than 50 years, TranSystems has committed to a mission of performing engineering and architectural planning, design, and construction solution services in a manner that is both safe and in compliance with all applicable regulatory and client requirements.
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As well as preparation of compliance and regulatory documentation for local (i.e. the Institutional Review Board), state and federal (ex. Responsible for general administrative work related to assigned study(ies), including but not limited to processing subject reimbursements and incentives, inventory and ordering supplies, organizing billing of services, etc.
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From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Recruit study participants by calling the database, attending company sponsored community events, posting flyers in schools, senior centers, supermarkets, and other establishments.
$20 - $22 an hourFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Two-Year College Degree or Completion of Specialized Course of Study at a Business or Trade School, or Completion of a Specialized and Extensive In-House Training or Apprenticeship Program. Knowledge of teller, member service, loan policies, understanding of office operations and function, and knowledge of legal and regulatory requirements.
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Experience in regulatory submissions (clinical study reports) presented to regulatory authorities a plus. Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias.
Full-timeRemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Under the supervision of a senior staff from the Biostatistics group, the incumbent will work closely with colleagues from Data Management, Statistical Programming, Clinical Development, Clinical Operations, Regulatory Affairs and Medical Affairs.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in the development of clinical strategy and the design of study protocols.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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This includes, but is not limited to, the following aspects of the project design and management:grading, utility management, stormwater management, sediment and erosion control, permits, and regulatory approval.
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Create and maintain IRB applications and regulatory binders for each study. The Sr. Research Program Coordinator will be responsible for the effective management of the research program and program staff to include clinical research and echocardiography laboratory activities, cardiac imaging project management, regulatory and data management portfolio, financial accounting oversight for sponsored accounts, grants and contracts management.
$40,900 - $71,600 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago
study regulatory jobs in Baltimore, MD
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