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Our client, a world-leading Pharmaceutical Company in New Brunswick, NJ. is currently looking for a Blackline Software Support Analyst to join their expanding team.
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Job Title: Sample Management Associate / LIMS / Pharma Manufacturing. Our client, a world-leading Pharmaceutical Company in Sanford, NC is currently looking for a Sample Management Associate to join their expanding team.
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Providing overall leadership and direction to the Quality Assurance and Regulatory Affairs McKesson 3PL Team. The Senior Director, QARA is principally responsible for the development and implementation of the Companys quality assurance program through the development and implementation of quality assurance and compliance standards via policies and procedures, training, auditing and monitoring, facilitating internal reporting, compliance-related investigations, and keeping Third Party Logistics VP of Quality Assurance & Regulatory Affairs informed on quality assurance and regulatory affairs matters.
$142,200 - $237,000 a yearExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Interact with R&D, Marketing, Regulatory, Medical and Scientific Affairs, and other global functions as well as senior leadership teams and global partners to apply advanced critical thinking to build strategic plans for new biomarker development, stakeholder management, and technology dissemination such as Real-World Evidence, ensuring benefit from the new capabilities and opportunities these enable.
$185,500 - $235,500 a yearFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Advanced degree in Science, Healthcare, or Regulatory/Clinical Affairs. The Clinical Affairs Director for Beckman Coulter Diagnostics is responsible for leading comprehensive global clinical trial strategies to support the complex Clinical Chemistry and Immunoassay Biomarker-Flywheel (Biomarker) program and for managing a multi-level team of clinical managers and clinical scientists/affairs associates.
$185,500 - $235,500 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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The JV is seeking an experienced and highly motivated individual to work with our team to support the Public/Government Relations (PR/GR) Manager and the Development Team to help contribute and drive the external affairs for Atlantic Shores Project 1as well as the community and government outreach strategies for the JV and its associated portfolio of mid-Atlantic offshore wind projects.
$100,013 - $166,688 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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You Will Assist the Vice President, Policy & Government Affairs (PGA) in developing and implementing federal legislative and regulatory advocacy efforts that advance SCAN's mission and federal policy positions.
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Senior Regulatory Affairs Specialist - Electrophysiology page is loaded Senior Regulatory Affairs Specialist - Electrophysiology Apply locations United States - Minnesota - Plymouth United States - Minnesota - St. Paul time type Full time posted on Posted 3 Days Ago job requisition id 31080311 Abbott is a global healthcare leader that helps people live more fully at all stages of life.
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Engages with cross-functional team members in Clinical Affairs, Operations Center of Excellence, Professional Affairs, Health Economics and Market Access, R&D, Regulatory, and Medical Safety and Infection Prevention & Control to review clinical evidence and to evaluate a product’s risk-benefit calculus.
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Reporting to the Managing Policy Director and Counsel and working closely with the VP of Policy & Programs, the Director will develop and implement policy and regulatory strategies in service of GRID’s mission to build community-powered solutions to advance economic and environmental justice through renewable energy.
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Reporting to President Darrell Williams, the VPBA&T serves as a critical member of his senior team and oversees: Auxiliary Services, Business Affairs, Comptroller, Conferences and Events, the Convocation Center, Human Resources, Office Services, Physical Plant, Police, and Purchasing.
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The President and community of The University of Southern Mississippi (USM, Southern Miss) invite inquiries, nominations and applications for the position of Provost and Senior Vice President for Academic Affairs.
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POSITION PURPOSE This position works directly with the Director of Government Affairs to formulate and implement PGE’s legislative and regulatory plans at the federal level. Ensure accurate maintenance of Government Affairs systems and procedures.
$101,925 - $169,875 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Monitor changes in relevant regulatory areas and provide education on those changes to business and operational personnel and compliance and legal affairs teams. Vanderbilt Health - Executive Search Team is conducting a national search for a Division Counsel - Compliance & Regulatory Attorney with a strong regulatory and compliance background, including expertise in federal and state fraud, waste and abuse laws and related regulations, Medicare and Medicaid (TennCare) regulations and conditions of participation, and clinical research compliance.
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The Campus Director of Academic Affairs is responsible for leading the delivery of quality student-centered, hands-on (active) learning. The Campus Director of Academic Affairs is responsible for maintaining high levels of academic quality and student satisfaction in order to retain and successfully graduate students, while operating in compliance with University policies and procedures as well as all state, federal and accrediting agency regulations.
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Title: regulatory affairs associate Company: Pioneer Data Systems
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