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Collaborate with study teams to successfully Initiate and manage local data generation activities (Protocol/synopsis development, Investigator selection & Investigator meetings, Study execution, results & publication, review of Investigator Sponsored Research (ISR) etc.
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Understanding of the nature of clinical data and concepts of IRT study configuration, resupply settings, blinding, privacy protection, and data quality/integrity standards. The IRT Lead will also partner with IGOT management for quality investigations, CAPA commitments and continuous improvements, SOP review and revision activities, support regulatory inspections, and limited duration teams where appropriate.
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Apex Systems is seeking a Clinical Research Coordinator to support data collection in the lab. ● Assist research team with Institutional Review Board (IRB) submission and compliance management.
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The incumbent assesses the request, conducts all necessary research such as verifying benefit coverage for the patient, and then creates the case (data entry) in Highmark's utilization management system for clinical review.
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Implements and coordinates contracted clinical trials, including startup, vendor management, subject recruitment, source development review, protocol training, conducting visits, data entry, query resolution, managing adverse events, and implementing new protocol amendments.
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Protocol Development, Case Report Form (CRF; review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Executes statistical activities for low to medium complexity studies including study design, protocol development, CRF review, SAP development, analysis files development, data surveillance review, statistical analysis accuracy validation, results interpretation and CSR input and review.
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Meets with the Clinical Research Associate at each scheduled monitoring visit and is available to complete queries or data clarifications in timely manner during these visits. Documents laboratory data and adverse reactions, presents this information to an investigator in a timely manner, and immediately notifies investigators, the Institutional Review Board and sponsor of any serious adverse events.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Experienced with writing, reports, agendas, data analysis, public health, grant writing, clinical research, project management, strategic planning, and portfolio analysis. Work with staff on to conceive, design and perform detailed analysis of the scientific landscape and/or administrative factors affecting research program priorities and performance in various scientific areas; Review scientific, administrative, and fiscal aspects of such grants, and evaluate them for scientific progress, programmatic relevance and merit.
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The Clinical Research Coordinator I will participate in clinical research activities related to the Mount Sinai Million project, a Mount Sinai Health System-wide initiative to generate genetic sequencing data on a highly diverse cohort of one million Mount Sinai patients.
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Our company is looking for qualified candidates to participate in paid national and local focus groups, clinical trials, and also market research studies. This is an excellent opportunity to supplement your income if you are a data entry clerk or anyone seeking a flexible part-time remote work from home job.
$30 - $35 an hourTemporaryExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts.
$82,800 - $157,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Write, edit, and review medical and scientific elements of clinical research, operational and regulatory documents, including but not limited to synopses, protocols, CRFs, informed consent templates, feasibility assessments statistical analysis plans, regulatory documents (eg, IND, MAA, NDA, PIP), key study plans, and clinical study reports to ensure accuracy, consistency with standard of care, logistical ease, and internal consistency.
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Our company is looking for qualified candidates to take part in paid national and local focus groups, clinical trials, and market research studies. Every month, we carefully curate and publish about 150-200 quality paid focus group, surveys and clinical trial studies.
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For most of our paid market research tasks, you can choose to participate either remotely or in person. Opinion Focus Panel LLC has been facilitating market research for over 7 years. Data entry clerk experience is not compulsory.
TemporaryRemoteExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
$82,800 - $157,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago
clinical research data review jobs in Hoboken, NJ
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