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Must have working knowledge of Fannie Mae/Freddie Mac and FHA/VA policies and guidelines, as well as, Regulatory Mortgage Compliance, state, federal, local government, private investors and insurers.
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Duties include ensuring personnel are properly registered to perform X-ray Service, Sales and Training; amending/renewing Radioactive Material Licenses and X-ray Registrations; maintaining records associated with Radiation Safety Programs; and assuring all regulatory required reports and submissions are accurate and filed on a timely basis.
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Ensure effective regulatory compliance to the NERC CIP. Knowledge and experience of application of NERC CIP in high voltage substation. Ensure effective regulatory compliance to the NERC CIP. Perform all SCADA, communication/HMI design and programming aspects for FACTS and HV substation.
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Proven experience in hematology/oncology drug development, designing and managing clinical trials (Ph 1b/II and Ph III) through investigator and regulatory interactions; experience with early-clinical development, including FIH and IND, is a plus.
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Firm Type: Law Firm, Experience: 5 Years, Job Overview: A law firm seeks a qualified Mid-Level to Senior Health Care Associate Attorney with 5-10 years of transactional and regulatory healthcare experience.
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Help us shape the online experience of high-profile initiatives for our clients, including the National Football League and the U.S. Department of Veterans Affairs. The web content strategist will work full time as part of a team of user experience (UX), web design, development, and search engine optimization professionals.
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This mission is accomplished through the proactive, fair and consistent enforcement of the state laws related to alcoholic beverage control, gambling, tobacco, controlled substances, and nuisance abatement, as well as other criminal and regulatory matters in the interest of health and public safety.
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This position is part of Quality and Regulatory Affairs located in Fargo, ND and will be fully remote. The Director of Global Regulatory Affairs will be responsible for developing and executing regulatory strategies for drug development and commercialization ensuring compliance with global regulations and standards across multiple markets.
$150,000 - $170,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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The QC AD Bioassay Scientist 2 ensures GMP compliant laboratory operations in accordance with regulatory guidelines. Supports regulatory requests and inspections. Serves as the QC Analytical Development Bioassay subject matter expert (SME) to author and review SOPs, transfer plans, protocols, and reports as part of the tech transfer process to onboard client programs.
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Our Internal Audit team advisesclients on process efficiency, fraud detection, operational quality, internal control, and regulatory compliance. Certifications including CPA, CDFM, CGFM, CFA, CIA.
$62,985 - $110,500 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Performs on-site Safety & OSHA branch regulatory inspections at each location three times annually following branch inspection checklist. Works with SWAT and transportation employees on maintaining proper documentation of DOT Driver/Vehicle Examination Reports and of any subsequent repairs and payments of citations.
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The Regulatory Affairs Specialist will assist in providing regulatory services to management for the Global Regulatory Affairs (GRA) group throughout the functional operations of improving entire drug development and commercialization process in areas including document authorship and review, preparation of applications for global submission, authorship and review to deficiency responses, and maintaining current regulatory practices and expectations.
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Responsible for reviewing the data management documentation, data management plan (DMP), CRF, study database specifications, data validation plan, edit check specifications, data transfer specifications, data issue logs, data review plans and ensures all documents follow study design and regulatory requirements.
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With a focus on providing talent for patient support, field/inside sales, medical device support, clinical support, and medical affairs our CSMS division has 10,000+ field professionals in more than 30 countries addressing physician and patient needs.
$24 an hourFull-timeExpandUpdated 2 months ago - UpvoteDownvoteShare Job
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Bachelor’s degree preferably in computer science, data science, regulatory affairs, business, organizational or compliance law, or financial services. Experience interacting with financial services regulatory bodies; preferably Office of the Comptroller of the Currency (OCC), Federal Reserve Board (FRB), FDIC, etc.
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regulatory affairs jobs Company: Jobget in Cary, NC
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