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Piper Companies is currently seeking a Regulatory Affairs Specialist, Cell & Gene Therapy for an opportunity in Philadelphia, Pennsylvania (PA), to join an innovative biotechnology company creating life-saving cell therapies.
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Deloitte Risk and Financial Advisory's Financial Services Industry (FSI) Risk, Data and Regulatory professionals help organizations identify the regulatory changes impacting their business and implement effective and efficient processes to manage regulatory, capital, liquidity and interest rate risks, respond to evolving regulatory environments and implement programs, measures, and tools to help clients with a specific focus on risk, data, and regulatory processes.
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The Regulatory Law Unit's Airport Division is seeking a licensed Pennsylvania Attorney to fill an Assistant City Solicitor or Deputy City Solicitor position. The attorney will work on a wide range of transactional and compliance matters handled by the Airports Division, including negotiating and drafting of contracts and advising the airport staff on legal and regulatory matters, as necessary, for the City to operate and develop its two airports.
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Job DescriptionThe Clinical Research Coordinator B/C will assist in oversight, execution, and regulatory compliance of human subject research for clinical research projects exploring investigational treatments and diagnostic tools relating to the care of patients with Epilepsy.
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Position Summary: Manages assigned aspects of the QAPI Program for Home Health to include compliance with Medicare Conditions of Participation (CoPs), and regulatory, and accreditation requirements.
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Audit operational areas and delegated vendors for compliance and ensure Jefferson Health Plans (JHP) is meeting applicable federal and state laws and regulations, and contractual requirements as set forth by all regulatory entities including but not limited to Pennsylvania State regulatory agencies (DHS, DOH and PID) and Centers for Medicare and Medicaid (CMS.
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Adheres to all requirements, expectations, guidelines, regulations and procedures outlined by the program, COMHAR, and all regulatory bodies (ex: CBH, OMHSAS, DBHIDS, NIAC, etc). Provides individual and group therapy to address addictive behaviors that complicate primary mental/behavioral health issues, using Evidence Based practices and approaches such as: CBT, DBT, Trauma Informed Care, Motivational Interviewing, IDDT, TAMAR, EMDR and Harm Reduction.
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Oversee the use of data automation and data analysis techniques to address regulatory requirements of SEVIS. The Assistant Director is responsible for identification and implementation of technical solutions to address issues that are discovered through data analysis.
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Document the psychological assessment, evidence-based, time efficient treatment interventions, and treatment plans in a timely and appropriate manner, to maintain thorough records in compliance with regulatory and insurance requirements.
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Biology), with 10+ years of relevant experience or a PhD with 4-6 years of relevant experience Must have demonstrated expertise in global, biologics regulatory CMC Sound understanding of molecular biology and cell culture.
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Responsibilities include but are not limited to; initial project development and space planning, creation & management of project budget and timelines, coordination of architects, engineers, consultants, contractors, vendors, and end users, obtaining necessary permits and regulatory approvals.
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Support the Program Specialist role across PA’s IDD programs to ensure regulatory compliance, standardization, and best-practices regarding ISP development/updates, SIS Process, Monthly/Quarterly documentation, Progress/Service Note templates, Health Review Screening Tool, Annual Assessments, and other ODP-mandates.
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Position Summary: This is an exciting opportunity to join Arcadium Lithium's Law Department as Assistant General Counsel, Global Finance and Regulatory Compliance. This role will report to Arcadium Lithium's Associate General Counsel and will serve as primary legal counsel to the company's Global Finance team and will support global regulatory compliance activities.
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Must be a law school graduate with an LLB or JD degree Must be admitted to the Pennsylvania Bar.5 or more years of experience working with laws and regulations related to litigation, commercial, energy, and/or regulatory law.
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Represents Jet Aviation as one company internally and externally with industry groups, regulatory bodies and the General Dynamics network. Represents Jet Aviation as one company internally and externally with industry groups, regulatory bodies and the General Dynamics network.
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regulatory job Title: regulatory affairs assistant Company: Abbott Laboratories in Philadelphia, PA
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