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Review upstream (prime contract) and downstream (purchase order & subcontract) change orders. Analyze data, review logs, and run reports in the Enterprise Planning & Controls software or other tools.
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Scope, direct, and review geotechnical engineering analyses and reporting for moderate to complex geotechnical and geo-environmental projects. Serve as technical lead on full-service design and construction services for geotechnical and geo-environmental engineering aspects of remediation and mining projects including landfills, slurry walls, sheet pile walls, sediment dredging, sediment capping, solidification and stabilization of contaminated soils and sludge, lagoon closures, industrial waste impoundments and mine site remediation.
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Create and validate mass spectrometry and chromatography parameters and methods for the quantitation of analytes using LC-MS and GC-MS. Write, review, and update SOPs and oversee method development and validation.
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Preparation of Schedule Projection (What-if) and Time Impact Analysis per Regional Project Control Manager AcceptancePreparation of Critical Path and Variance analysis reports for review with Regional Project Control ManagerCoordinate, develop WBS dictionary with Project Accountant Manager.
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Review and report customer DNA sequencing data. We are a market leader in automated bio sample management solutions and genomic services across areas such as drug development, clinical and advanced cell therapies for the industry's top pharmaceutical, biotech, academic and healthcare institutions globally.
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Review/approve creation/modifications to Master Stability Protocols (MSP) and Study-Specific Protocols (SSP), batch-specific enrollment documentation, and LIMS stability studies. Activities include (but not limited to) those associated with developing product stability strategy; stability data analysis/trending; and preparation, review and approval of stability protocols, reports and regulatory filings.
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Review MRP/demand planning requirements and understand component forecasting and usage and ensure supplier understanding of PO requirements for long-term product availability. Monitor KPI indicators such supplier on time delivery, purchase order confirmations, inventory cycle count accuracy, and Purchase Price Variance (PPV.
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Program data review and quality checking programs ensuring delivery of high-quality output for clients. Understanding of the clinical trial processes including common data standards (CDISC) and statistical outputs (SAS.
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Maintain and review Plasma center personnel training documents to ensure documents comply with CSL procedures, SOP's, CLIA/COLA and other applicable requirements. Perform final QA review and release for all shipment and associated documents, to ensure shipment meets customer specifications.
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Knowledge of milliman and/or interqual criteria, utilization review, discharge planning and case management. Knowledge of milliman and/or interqual criteria, utilization review, discharge planning and case management.
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I.e., H&P, Labs) etc Ascertains the need for pre-certification or pre-authorization Obtains insurance information Receives films of prior studies, has physician review films before booking procedure to ensure correct modality Aides in activities which help the department.
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Must be prepared to discuss output with Vice President of Operations and Director of Regional Sales at quarterly review. Job Title: Operations Supervisor Advertising Title: Req #: 11962 Company: Ward Trucking, LLC Job Code: SVCTROPS Location: South Plainfield Employment Status: Full Time City: South Plainfield Area of Interest: Manager State: NJ Rate of Pay: Competitive Salary and Benefits Package.
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Review and ensure accurate and complete resolution of issues as they arise and escalates concerns, resource constraints, and needs accordinglyRequired Skills/Abilities: B.S. degree environmental, science preferredMinimum of 3 years of experiencePrior EHS Incident and/or Project Coordinator experience requiredProficient with Microsoft Suite (Outlook, Word, Excel, Power Point)Experience with incidents and/or learning systems database (e.g., Enablon, Success Factors, Compliance Wire, etc.
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Under the direction of the applicable management, the Lead Clinical Data Manager (LCDM) is responsible for executing end-to-end data management activities pertaining to clinical trials, including but not limited to data management tool and system development, validation and maintenance, data collection, data integrity review and reconciliation, query management, medical coding, and database lock preparation, in compliance with Sponsor Standard Operating Procedures (SOPs) and ICH-GCP guidelines.
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Conduct a brief review of prior FTC agreement service plan, family history in CONNECTIONS and hard case record prior to the FTC.Conduct & participate in debrief meetings prior to FTC and when applicable (a debrief might be required) immediately after an FTC.Ensure debrief meetings occur consistently with Case Planner, Trauma Counselor and/or unit Clinical Supervisor, to consult about any unresolved questions and/or concerns.
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review job in Woodbridge, NJ
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