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The Specialist will assist with import-related documentation, product classification support, PGA applicability, FTA & GSP review, C-TPAT Program administration, and other risk elements such as ADD/CVD applicability.
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During this individual supervision a chart review should be completed using the updated Utilization Review sheet with particular attention paid to whether or not a PGP exists to cover the time period since the last CBH review.
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These responsibilities include, but are not limited to, all concurrent utilization review activities as it relates to telephonic review, all clinical pre-certification responsibilities, all retrospective review responsibilities and all insurance company and business office concurrent determination follow-up and communication.
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Reporting to the Regulatory Affairs Manager, the Regulatory Affairs Specialist will, with minimal supervision, prepare and process all regulatory documentation through the IRB, CTSRMC, FDA and all applicable regulatory review committees- including new submissions, continuing reviews, amendments, adverse events, and reportable events.
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Collaborate with Project Control to review purchase requisitions in Deltek Costpoint prior to approval for procurements. Review prime contract to determine proper flow down of clauses to subcontractor.
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Summary: As a Senior Project Manager in the Antitrust Practice Group (Managed Review), you will oversee challenging and fast paced regulatory or litigation antitrust matters for our clients. Background of 5+ years in Managed Review with a concentration in Second Request, Antitrust litigation and other high-volume cases highly preferred.
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Review claims and loss trends to initiate loss mitigation efforts. professional designations such as Certified Safety Professional (CSP), Certified Fire Protection Specialist (CFPS), Certified Industrial Hygienist (CIH), Occupational Hygiene and Safety Technician (OHST), Chartered Property Casualty Underwriter (CPCU), Associate in Risk Management (ARM) or Certified Risk Manager (CRM.
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Reporting to the Regulatory Affairs Research Teams Manager, the Regulatory Affairs Specialist will, with minimal supervision, prepare and process all regulatory documentation through the IRB, CTSRMC, FDA and all applicable regulatory review committees- including new submissions, continuing reviews, amendments, adverse events, and reportable events.
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Duties: Draft and review venture capital investment documents, ensuring accuracy and compliance. Strong academics, excellent writing skills (preferably law review or journal experience), and PA Bar admission or the ability to waive in are essential for this role.
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Education Requirements Graduate of a JRCERT (Joint Review Committee on Education in Radiologic Technology) accredited dosimetry program; OR Licensed Radiation Therapist/Radiological Technician with additional dosimetry training.
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Ability to development/oversee Data Management specific documentation including but not limited to the eCRF specifications, eCRF completion guidelines, edit check specifications, validation documents, DMP and DRP (Data Review Plan.
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Lead monthly P&L review meeting with CTO and CIO and assemble monthly P&L report to be presented in that meeting. Review and audit invoices, identify errors, log disputes with vendors when necessary, and see through to resolution.
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Lead, develop, assist with, and review traffic impact studies, highway occupancy permits, specifications, signal design and plans, maintenance and protection of traffic and signing plans, PS&E packages, and reports.
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General experience in Patient Safety Activity(ies) such as RCA, FMEA, Peer Review, Rapid Cycle PDSA, Performance Improvement Methodologies and tools (Six Sigma, Lean, etc.) Using just culture principals will participate in or lead patient safety processes (FMEA, RCA, adverse event investigation) and review of attorney correspondence as directed.
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This position is responsible for ICD-10 Coding and OASIS Review, quality assurance, accuracy and overall integrity of the clinical records and documentation completed by Clinical staff. This position is responsible for ICD-10 Coding and OASIS Review, quality assurance, accuracy and overall integrity of the clinical records and documentation completed by Clinical staff.
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review job Company: Nrg in Camden, NJ
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