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The Product Safety & Regulatory Compliance Team is seeking a Regulatory Affairs Manager to join our team. Experience working in regulatory compliance, chemical control, regulatory affairs, environmental, laboratory or product safety in the agriculture industry.
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Deep understanding of AML and KYC counterparty risk identification and mitigation principles, including BSA/AML, CDD/EDD, JMLSG, Sanctions, Fincen CDD, Travel Rule, and TMS global regulatory requirements.
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Assist in the preparatory work prior to and during AML/BSA/OFAC internal audits and regulatory examinations. As a Senior Financial Crimes Governance Specialist you would support the AML Compliance function by executing various processes that maintain compliance with regulatory requirements and the firm’s AML / CTF Program.
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Audit and Regulatory Review Support: Assist model validation manager in gathering and providing materials requested by internal audit and regulators, drafting responses to questions, and defending validations in exams.
$160,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The Vice President provides leadership to all areas within Student Affairs including Residence Life, Student Activities, Campus Police/Security, Counseling Center/ADA Compliance, Counselors, and Intramurals.
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ResponsibilitiesUnder the general direction of the Associate Vice Chancellor, Strategic Communications and Brand Marketing, the Senior Director, Media Relations and Public Affairs will:-Build and maintain positive, constructive relationships with key contacts across the Chancellor’s Office and the CSU to aid in fulfilling media inquiries.
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Daiichi Sankyo, Inc. (DSI) is currently seeking a Medical Science Liaison (MSL) to join the Field Medical Affairs Team. The MSL develops ongoing professional relationships with national and regional healthcare opinion leaders and other healthcare professionals to provide medical and scientific support for Daiichi Sankyo, Inc. (DSI) initiatives in selected therapeutic areas.
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Offering expert guidance from concept-through-commercialization, including product design and engineering, preclinical and clinical development, data management, market access, regulatory affairs and quality assurance, Veranex enables accelerated speed to market, controlled development costs, development risk mitigation, and accelerated market viability assessment.
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Work in the Global Rare Diseases, Regulatory Affairs Ad Promo function for the United States, with additional duties in Canada. Minimum 5 years Pharmaceutical/Biotechnology industry experience, at least 3 years Regulatory Affairs and advertising and promotion review and approval experience with marketed prescription drugs.
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HDR is looking for Senior Dam Safety Engineers and/or Federal Energy Regulatory Commission (FERC) approved Independent Consultants (IC) in multiple locations across the country to join our thriving and growing Hydropower Practice.
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Provides in house legal counsel in the WakeMed Office of Legal Affairs and reports to the Vice President and Chief Legal Officer CLO or other attorney in the WakeMed Office of Legal Affairs.
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MedPro is one of the largest recruiters of therapists and nurses from outside the U.S. MedPro currently has contracts with numerous organizations to service a multitude of facilities in the U.S. The company counts among its clients prominent healthcare facilities and organizations such as the Department of Veterans Affairs,HCA, University of Miami Hospital, and Tenet Healthcare.
$1,841.98 a weekFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Offering expert guidance from concept-through-commercialization, including product design and engineering, preclinical and clinical development, data management, market access, regulatory affairs, and quality assurance, our client enables accelerated speed to market, controlled development costs, development risk mitigation, and accelerated market viability assessment.
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Reporting to the Chief External Affairs Officer (CXO), the Grant Program Specialist will research, identify, define, and develop funding sources to support existing and planned program activities as well as lead the development, writing, and submission of grant proposals to private and family foundation funders.
$78,000 a yearFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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You will successfully interpret and advise on a clinical trial protocol design with respect to supplies, in conjunction with key Clinical Operations, Regulatory Affairs and Quality Assurance colleagues.
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regulatory affairs jobs Title: sr Company: Planet Pharma in Garner, NC
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