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As a member of the Internal Audit department, this position is responsible to review activities in assigned areas to determine the nature of operations and the adequacy of the system of controls to achieve Company objectives.
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In addition to study level activities, the clinician medical monitor may participate in standing committees, review compounds for potential in-licensing, including performance of due diligence reviews, and provide assistance to new business development on market opportunities and the target product profile.
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Perform additional construction management activities, including development procurement - construction schedules, construction subcontract scopes, review of subcontract terms and conditions, performance of constructability and value engineering reviews, construction estimating and schedule reviews, and project construction performance presentation.
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The Medical Claims Adjuster - Remote is responsible for the review, investigation, decision making, and processing of production claim types, and all related claim functions and activities.
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As the Production Scheduler, you will assist in coordinating the day-to-day activities of a team of production workers to ensure that manufacturing operations run according to established production specifications and schedules; volume, cost, and wastage targets; and quality standards.
$31.5 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Quality Assurance Associate III is responsible for performing Quality Assurance activities within minimal supervision of daily tasks in support of Quality Systems and/or client procedures including but not limited to document management, issuance, review and approval of batch records, SOPs, Qualification and Validation Reports; review of QC data; perform material releases and final product releases; review of Deviations as well as assists Quality management with department needs.
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Coordinate activities with the Berkshire Hathaway Internal Audit group and assist in Berkshire/E&Y internal audit reviews as required. Conduct financial, operational and control review of third parties including sales agreements, freight claims processors, co-op claims processors, etc.
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Contributes to or executes activities for estimation, planning, and review of technical tasks in support of overall project acquisition, negotiation, planning and management (partly before PM100.
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Preparation, Review and filing of all post marketing activities which include, timely submission of Annual Reports, CPP, release of detained products at customs etc. Review and approve Prototype formulation during early drug development stages to be compliant with Inactive Ingredient Database and FDA guideline.
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Supports customer remotely and onsite, and provides 2nd and 3rd level user support in case of arising issues. Completes broad scope of technical tasks including installation/commissioning, maintenance and evaluation of customers equipment and systems among others (after PM100.
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Graduate of an accredited (Accreditation Review Committee for Physician Assistant Programs ARC-PA) program, required. Participates in performance improvement, research, and educational activities.
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Conduct performance improvement activities regarding coding accuracy, completeness, data quality and integrity; identify issues in correct sequencing of codes and assignment of grouper payment methodology,Collaborate with physician, nursing and other clinical staff and review agencies on responses to denials, and other issues and to obtain clarification on documentation of clinical care.
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Conducts medical review and interpretation of efficacy and safety data from clinical trials; this may include delivery of top-line report in collaboration with study statistician, and delivery of clinical study report in collaboration with medical writer and accountable for overall quality and timeliness of analysis and reporting.
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Works closely with clinicians, statistician, and publication managers to generate and QC outputs for publications; reviews publication (abstract/ manuscripts) to ensure accuracy, quality and soundness of statistical methodologies; coordinates internal resource utilization for publication and generate activities metrics for management review.
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Perform activities associated with disposition of raw materials and product (e.g., receipt, inspection, document review, shipping, etc. The QA Specialist performs activities in support of dispositioning product while ensuring compliance with Quality Assurance (QA) policies and procedures, cGMPs, SOPs, and Regeneron Standard Requirement Documents.
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review activities jobs in Spring Valley, NY
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