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The Manager, UM Regulatory & Compliance - CCA is responsible for the coordination, implementation, and oversight of the IEHP’s overall Utilization Management Out-Patient Operations departmental clinical and operational compliance with regulatory requirements and quality assurance initiatives related to utilization management out-patient activities (e.g., Prior Authorization, UM Call Center operations.
$56.85 - $91.64 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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A well-established Renewable Energy Company is looking to add on a Regulatory Compliance Specialist-NERC/CIP. This role will serve as a primary liaison with regulatory and reliability entities, including FERC, NERC, regional entities (MRO, NPCC, RFC, SPP RE, TRE & WECC), Canadian authorities (AESO, IESO, MSA & NB Power), and others relevant to renewable generation assets and control centers.
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Identifies regulatory compliance gaps and mentors leadership in developing appropriate plans to address and close the gaps to achieve outcomes, promote safe practices and achieve sustainable compliance with regulatory standards; works collaboratively on VMFH annual intra-cycle monitoring of compliance with TJC standards, including with identified opportunities for improvement and corrective action plans.
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Data Governance and Compliance: Assist in data governance initiatives, ensuring compliance with data security, privacy, and regulatory requirements. Dashboard Development, data analysis & Visualization: Lead the design and development of dashboards utilizing PowerBI that provide real-time insights into Treasury operations, supporting data-driven decision-making.
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Proficiency with drug safety databases (i.e., Argus), electronic data capture (EDC) systems, Medical Dictionary for Regulatory Activities (MedDRA) and World Health Organization (WHO) Drug dictionary coding.
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Extensive experience in late-phase drug product development and commercial development with CMC regulatory filings for the US (NDA), Europe (MAA), Japan, and China. Collaborate with cross-functional teams (process R&D, analytical development, supply chain, quality, clinical, regulatory, DMPK, and tox) to meet CMC and program goals.
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Must have ability and willingness to research regulatory compliance matters, including Federal Acquisition Regulations (FAR) We are looking for a Finance Manager, Government Compliance to join our growing team.
$90,000 - $130,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Assist Radiation Safety Officer (RSO) with management of nuclear gauges to ensure compliance with regulatory requirements. Assist with questions regarding regulatory compliance with OSHA, MSHA, EPA, CDC/NIH, and state and local regulations.
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10+ years of experience in site development, environmental review and analysis, permitting, compliance, and regulatory analysis specifically for fossil and renewable power generation and storage facilities.
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Provides policy guidance and assistance with all aspects of proposal development, administrative forms, sponsor-required certifications and representations, and compliance requirements. They are a primary resource for providing guidance and oversight on issues related to fiscal, administrative and regulatory management of a portfolio of grants, contracts and sponsored programs from award receipt through closeout.
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Keeps abreast of and ensures compliance with regulatory practices (e.g. FDA, EMA, and ICH guidance and recommendations) and industry data standards (e.g. CDISC). Leads biopharma related business development activities on behalf of the global biostatistics department including but not limited to proposal, budget development, and bid defense support.
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As a Licensed Drug & Alcohol Counselor (LADC) at our Residential Treatment Center, counselors will play an important role in the delivery of treatment services by working hand in hand with our peer support recovery specialists, Suboxone providers, and medication management.
$70,000 - $72,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Lead the independent medical education (IME) function and ensure successful development and execution of the annual medical education strategy that leverages innovation, program impact, collaboration, business/therapeutic area alignment, and compliance to address the identified educational objectives for healthcare professionals and patients.
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Week)Frontage Laboratories Inc. is an award winning, publicly listed (HKSE), full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, and China, and growing over 30% YOY. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.
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Develop strategies and tactics that follow local, regional, and national compliance and regulatory guidelines inclusive of related medical education policies and procedures that may impact Genmab strategy and support (e.g., provider accreditation status changes via the ACCME, government programs such as MACRA/MIPS that may affect IME.
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drug development regulatory compliance jobs Title: manager program
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