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Ensures a department commitment to cultural affairs and ensures all direct reports have a cultural affairs component to his or her planning document as a measurable. Opportunity for enhanced clinical training through conferences, consultation groups, and trainings on EBPs (Trauma Focused Cognitive Behavioral Therapy, DBT, Motivational Interviewing, Substance Use Disorders, EMDR.
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May develop Standard Operating Procedures (SOPs) and Work Instructions (WIs) as directed by the Senior Director CMC Regulatory Affairs. Prior pharmaceutical industry experience and a minimum of 8 years in CMC Regulatory Affairs for Associate Director.
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As part of the Regulatory Affairs CMC team, you will report to the Executive Director and Head, CMC Regulatory Affairs Pharmaceuticals. Join Takeda as a Senior Director, GRA Pharmaceuticals- Small Molecule where you will establish collaboration with Global CMC teams and leadership through networks and enable CMC regulatory teams success in meeting goals/objectives.
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This position provides an opportunity to join the US Global Regulatory Policy & Advisory team as a subject matter expert, with a focus on providing policy guidance on the Fundamental Review of the Trading Book (‘FRTB’) / new Market Risk capital requirements within the US Agencies’ proposed adoption of the ‘Basel III Endgame.
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To do these effectively, the Analyst III – Policy & Regulatory Operations must have a demonstrated understanding of IEHP business operations and responsibilities of various departments in Health Services, Quality Systems, Provider Services, and Member Services; subject matter expertise of these departments’ policies and procedures and the regulations that drive their business operations and demonstrated ability to effectively and consistently manage multiple projects and priorities concurrently.
$80,059.2 - $106,059.2 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Under the direction of the Associate Dean for Academic Affairs, assists the Sr. Academic Program Coordinator with the studio lottery process. This position reports directly to the Associate Dean for Academic Affairs and works collaboratively with the Sr. Academic Program Coordinator within the Academic Affairs team.
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The Director will advise and work closely with colleagues in creative, production, finance, marketing, publicity, consumer products, as well as with Business and Legal Affairs in other departments.
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The Assistant Program Director is responsible to assist the Program Director and the Campus Dean of Academic Affairs with the fiscal well-being of the program as it relates to education and helping to maintain/grow enrollment.
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Similar Jobs (5) Global Trade & Shopper Lead - Allegra locations 2 Locations time type Full time posted on Posted 30+ Days Ago Medical Safety Head, PV (CHC) locations 3 Locations time type Full time posted on Posted 30+ Days Ago US Regulatory Affairs Lead, OTC Brands locations Bridgewater, NJ time type Full time posted on Posted 3 Days Ago.
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POSITION SUMMARY Reporting to the Managing Counsel, Health Affairs, Privacy & Data Protection Law, the Principal Counsel - Health Regulatory provides primary legal support to the University's medical centers and health sciences schools on complex and high impact healthcare regulatory analysis.
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Leading new business architecture required to support the Regulatory Capital computation per the Federal Reserve Bank Basel III requirements across the IHC. Extensive experience with Federal Reserve Bank Basel III regulatory Capital requirements, preferably at a Large FBO.
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Strategic Communications and Public Affairs (StratComm) serves as the official voice of San Diego State University and shares the President's vision, values and priorities while articulating a unified message about the university's unique story.
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Korn Ferry has partnered with an established 503A compounding pharmacy company on its search for a Vice President of Government Affairs, reporting to the CEO/Deputy General Counsel. Deep understanding of pharmacy industry, including compounding pharmacy, outsourcing facilities, supply chain & regulatory environment.
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Consistent adherence to field and corporate policies and Global Medical Scientific Affairs (GMSA) strategy, including field standard operating procedures (SOPs), Good Clinical Practice (GCP) guidelines, and administrative/operational responsibilities.
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This is what you will do:The Senior Director of Regulatory Affairs Chemistry, Manufacturing, and Controls (RCMC) will provide strategic as well as operational leadership of global CMC activities related to Cell & Gene Therapy (GCT) leading to successful registration and life-cycle management of unique and technologically complex products.
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regulatory affairs jobs Title: sr director Company: Merck
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