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State Government Affairs (CSGA) develops and implements strategies for. Chief of State Government Affairs. Ability to quickly analyze, evaluate, and respond to legislative and regulatory proposals, complex data, and other information on educational issues and legislation.
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The Clinical Supervisor is responsible for maintaining OASAS regulatory compliance and assuring that programs operate in accordance with VIP Community Services organizational standards. Qualified Mental Health Professional (e.g., LCSW, LMSW, LMHC, CRC, Ph. D., MSN, CASAC, etc.
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Must be and remain compliant with any and all regulatory requirements for working in the cannabis industry. The Dispensary Associate is responsible for guiding customers through the cannabis purchasing experience, making informed recommendations based on customer's desired outcomes, provide informed and accurate descriptions of our products, and operate with a high level of accuracy in a fast-paced environment.
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To provide oversight and guidance to ensure the eTMF system aligns with Eisai TMF vision and transformation initiative and is compliant with ICH-GCP and regulatory requirements. This includes overseeing the daily global eTMF system related activities relating to clinical study Trial Master Files (TMF), ensuring regulatory inspection-readiness and compliance with applicable laws and regulations.
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The risk landscape is continuously changing due to market volatility, geopolitical crises, widespread economic changes, regulatory reforms, and cyber threats. As a member of Risk Technology, you will help our clients assess, design/architect, and implement technology solutions to optimize their risk and compliance programs across risk disciplines (e.g., integrated risk management, enterprise risk management, IT risk management, cyber risk management, third party risk management, internal controls, compliance, internal audit.
$108,700 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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.
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Their practice areas includes banking and finance, litigation, media and technology, private equity, construction, bankruptcy, regulatory affairs, tax, trusts and estates, employment, environmental, health care, intellectual property, information security, public finance, real estate, disaster recovery claims and corporate travel.
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5 year prior experience in regulatory affairs within the dietary supplements or food industry, especially experience with an ingredient supplier is highly preferred. o Lead and execute regulatory affairs on customer documentation requests.
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The Model Risk Manager will also be involved in supporting the remediation of audit issues and/or regulatory feedback related to model risk controls. Banking experience in credit, capital markets, asset liability management, financial reporting, regulatory reporting, or operational risk areas.
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Certified Anti-Money Laundering Specialists (CAMS), Certified Internal Auditor (CIA), Certified Information Systems Analyst (CISA), Certified Regulatory Compliance Manager (CRCM) or other relevant professional certification.
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You will work closely with members of the firm's lines of business, Legal Department, Global Government Relations and Office of Regulatory Affairs to help coordinate the firm's response to proposed rules and regulations.
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Guides, directs and evaluates (1) Associate General Counsel, (3) Lease Administration Department (1) Senior Paralegals and, (2) Scientific & Regulatory Affairs Department. Provide guidance to Scientific and Regulatory Affairs on regulatory issues related to both product and procedures, including label safety, use of third party literature, and training documentation.
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At least 5+ years’ experience in working at an asset manager (preferably within AML, KYC and/or Regulatory Management) The ideal candidate will coordinate and execute regulatory filings, oversee Lord Abbett’s AML and financial crimes program, and identify and monitor for suspicious activities as they relate to AML and financial crimes.
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This role will supervise the GOLCS Manager of External Affairs. The Network Director of Marketing, Communications, and External Affairs will report directly to the Chief Strategy Officer.
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Keywords: regulatory specialist, clinical research, oncology, oncology clinical research, oncology regulatory specialist, clinical research coordinator, clinical research associate, oncology clinical research coordinator, oncology clinical research associate.
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regulatory affairs jobs Title: regulatory affairs manager Company: Baxter in Nutley, NJ
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