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New Business Review Supervision: Oversee the review process for new variable annuity, direct mutual fund, and all other Broker-Dealer business, ensuring they meet all compliance and regulatory standards before implementation.
$90,000 - $105,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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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Strong understanding of the regulatory environment for electronic money institutions, including the Payment Services Regulations (PSR), the Electronic Money Regulations (EMR), AML/CFT (Anti-Money Laundering/Countering Financing of Terrorism) regulations, JMLSG and FATF guidance, FCA Handbook.
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The Qualified Medication Aide sets up, administers, and records certain prescribed medications for residents in the facility under the supervision of a licensed nurse and as allowed by State regulatory agencies.
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The incumbent functions independently under minimal supervision, following FDA, Good Clinical Practice, IRB, NIH, NCI, NSF and/or other regulatory agency guidelines and seeking council from the Principal Investigator or manager as necessary.
$22.88 - $38.31 an hourFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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The Care manager works under the supervision of the Regional Director- Patent Centered Care Management to support the objectives of UVM Health Network - CVPH and the Medical Home. Responsible to identify at-risk patients and develop plan of care based on risk and patient goals to meet individual health needs through communication and assisting with access to resources to promote quality, cost-effective outcomes across the continuum of care.
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The Certified Occupational Therapy Assistant (COTA) is a skilled technical worker who performs direct resident care activities under the clinical supervision of the Occupational Therapist. Act in compliance with Heritage Healthcare's regulatory and professional standards and guidelines.
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Perform duties in an independent manner and recognizes situations where direct supervision is needed; willingly helping others. Certified Occupational Therapy Assistant (COTA) - PRN "as needed.
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The Captive Insurance Director of the Insurance Division is responsible for implementation and administration of new regulatory responsibilities enacted by the Iowa State Legislature in Senate File 549 (Iowa Code chapter 521J); The legislature established the Captive Insurance Regulatory and Supervision (CIRS) fund established in the state treasury under the control and supervision of the division.
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We encourage you to take the time to explore the opportunity to advance your career at Freeport-McMoRan. Description Works under limited supervision executing both long-term strategies and daily decisions for Freeport-McMoRan's North America operation's retail utility partners and affiliates.
$118,000 - $165,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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A Polysomnographic Technologist works under the general supervision of the clinical director (MD) or designee to provide comprehensive evaluation and treatment of sleep disorders. Performs all interventions/procedures within job scope and specific field of specialty in accordance with standards of care, policies & procedures, regulatory guidelines, and role specific competencies specifically: Routine, non-routine and complex recordings such as CPAP, Bi-level, split night studies, seizure studies, REM behavior studies, MSLT testing, scoring all records, routine PSG recordings & Oxygen Titrations.
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Document interpretation and conclusion of regulatory rules, specifically issued by the Federal Reserve Board, OCC (inclusive of the Interagency Guidance), Basel Committee on Bank Supervision and U.S. Securities and Exchange Commission, IIB, BPI etc.
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Ensures regular QA and calibration checks are performed as required on all dosimetry, x-ray, imaging, Nuclear Medicine and radiation therapy equipment throughout the System ensuring compliance with all regulatory requirements and State and National standards.
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Provide regulatory writing expertise, leadership, project management support, supervision of RSW resources, and strategic input on document preparation and submission for one or more compounds and/or projects within a TA. Ensures that documents authored by RSW are of high quality and are submission ready prior to submission to health authorities.
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UMMS is currently seeking a Compliance Auditor at our corporate office in Linthicum, MD. General Summary Under general supervision, ensures that compliance initiatives are met for all the University of Maryland Medical System (UMMS) Member Organizations.
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