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Professional accreditation such as a Certified Regulatory Compliance Manager (CRCM), Certified Internal Auditor (CIA), Certified Risk Professional (CRP), and Certified Anti-Money Laundering Specialist (CAMS) is preferred.
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The Assistant Dean, Academic affairs works under administrative review of the SPH Dean. This position is responsible for academic program planning, course scheduling, graduation, experiential learning, institutional effectiveness and may be required to represent the School of Public Health (SPH) and the dean's office in various campus committees and work groups as directed.
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The Microbiology Manager serves as a subject matter expert (SME) for regulatory and corporate audits and for technical support for Memphis in the areas of cleanroom control/validation, product sterilization and microbiological control.
$105,000 - $115,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Chief Medical Affairs Office's Real-World Evidence (RWE) Platform is responsible for establishing global scientific leadership and stature through the generation of integrated, end-to-end observational real-world evidence serving all therapeutic areas from proof of concept (POC) trials through LOE for priority pipeline candidates, pipeline supplementation through business development, and marketed inline products.
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Maximus will comply with regulatory minimum wage rates and exempt salary thresholds in all instances. We are seeking a Senior SAP BASIS Administrator to join our team supporting our Internal Revenue Service (IRS) client.
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Clinical RN Director Join Our Team as a Clinical Director at Gastro One/One GI Are you a dedicated and experienced healthcare professional looking for a leadership role in a dynamic and innovative organization.
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The QA Manager is the lead person for Pharmaceutical/Healthcare Operationsfrom a Compliance, Regulatory and Quality compliance perspective. QA Manager must have a clear understanding of FDA GMP, WHO GMP/GDP/GSP EUGDP, DSCSA, VAWD, and state regulations regarding distribution ofpharmaceutical products, state medical device regulatory requirements, and DEAand state regulatory requirements for controlled substances storage &distribution practices.
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With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide.
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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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Our global chemical client has an Environmental Leader opening in the EHS Group, involved with plant site regulatory and compliance in the areas of reclamation, water quality, chemical and waste management, air quality and environmental management systems.
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Knowledge of regulatory affairs, customs or other business areas of logistics. With expert teammates staffing more than 100 worldwide locations in Asia, Europe, India, and North America, AITs full-service options also include customs clearance, warehouse management and white glove services.
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The Sr. Regulatory Reporting Analyst will report to the Sr. Regulatory Reporting Compliance Manager and will work closely with the Lines of Business, IT, Compliance, Legal, and other risk partners in the development and execution of the Fair and Responsible Banking program.
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Operational management of clinical and non-clinical departments including but not limited to: Nursing, Admissions, Business Development, Process Improvement, Finance, Clinical Services, Regulatory Affairs that effectively drive patient care outcomesEnsure hospital quality metrics are achieved through sound clinical processes following accreditation and regulatory agency guidelines.
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Previous RWE experience in medical or clinical development, and interactions with regulatory authorities is desirable. US medical affairs, marketing, market access global value and access teams, commercial.
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The Sr. EHS Manager will lead the environmental, health, and workplace safety programs for multiple plants within this fast-paced, heavily-automated manufacturing organization, working cross-functionally with the operations management, human resources, safety, and security teams to ensure a safe workplace and full regulatory compliance of the organization's safety, health, and environmental programs.
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regulatory affairs jobs Title: director clinical lead in Memphis, TN
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