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Within Global Regulatory Affairs, our Chemistry, Manufacturing and Controls (CMC) organization provides regulatory leadership to CMC development teams and the Pharma Supply Chain organization to enable approval of new medicines and uninterrupted supply of our medicines to patients.
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The Professional Development Coordinator is one of eight regular, full-time staff members in the Graduate Student Affairs unit: an associate dean who leads the unit, three assistant deans, two senior program coordinators, and two program coordinators.
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QualificationsTo be considered for this role, you’ll require a minimum of 5 years of professional experience in relevant field of healthcare products or related activities e.g.:Work in medical devices industry and/or in vitro diagnostic devices(preferred) or closely related industries (e.g., pharmaceutical industry) such as research and development, manufacturing, quality management, regulatory affairs.
$103,500 - $170,800 a yearFull-timeRemoteExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Equally, we seek to deepen our understanding of the rapidly evolving molecular diagnostics landscape in NA. To achieve these objectives, the Medical Affairs Director will formulate a strategy specifically tailored for NA, aimed at bolstering our Division's growth in the fields of pathology and oncology.
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DEPARTMENTAL PREFERENCES Education/Training Master’s degree is required, preferably in student affairs, public health, health and wellness or a similar program. It encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh Hospital, Duke Primary Care, Private Diagnostic Clinic, Duke Home and Hospice, Duke Health and Wellness, and multiple affiliations.
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As academic officers of Trinity College of Arts and Sciences, Academic Deans report to the Dean of Academic Affairs and serve under the leadership of the appointed Senior Associate Dean. They are an integral member of the College Deans Staff and serve on College and University committees as requested by the Dean of Academic Affairs.
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This role helps develop the medical strategy and executes Medical Affairs tactics for a GSK Key Asset. Experience working in medical affairs accountabilities, evidence generation, external engagement and provider internal advice.
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This position interacts with departments throughout the organization including but not limited to Quality, Clinical Laboratory Operations, Technical Operations, Regulatory Affairs, Compliance, Program Management, Clinical Affairs, Supply Chain, Manufacturing, and Research & Development.
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Represent Global CMC Regulatory advising teams on global regulations and guidelines and providing strategic direction to cross-functional matrix project teams on medical device and drug/device combination product related topics.
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The Regulatory Affairs Manager is responsible for coordinating the regulatory activities for projects including new products and life cycle management. Supports regulatory compliance to ISO, FDA, and other worldwide regulatory requirements as appropriate through customer complaints, internal audits and training systems.
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In addition, registries or other vendor-run research studies within medical affairs may be managed by the HEOR employee. Responsibilities include, but are not limited to the following: ● Provides strategic planning, design input, and implementation of health outcomes programs ● Oversees and manages vendors conducting registries, outcomes, and pharmacoeconomic research within Medical Affairs ● Performs statistical analysis and complete data management using SAS, or similar, statistical software) ● Works with internal teams.
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The BHIP Social Worker is a professional Social Worker assigned to Mental Health Clinics within the Veterans Affairs Health Care System including outpatient clinics at Hillandale and Community-Based Outpatient Clinics located in Raleigh, Greenville and Morehead City.
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The Institute for Medical Research (IMR), a private nonprofit organization that conducts cutting edge research for the Durham Veterans Affairs Health Care System (DVAHCS), seeks to hire a Research Team Lead. The successful candidate will be employed by the Dr. Stephen Freedland, a nationally recognized leader in urology and urologic oncology research.
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Participation in the vaccination programs may be required for all Department of Veterans Affairs Health Care Workers Without Compensation (WOC) appointments. The Institute for Medical Research (IMR), an affiliate of the Durham VA Health Care System (DVAHCS), is looking for a full-time Administrative Manager to develop and oversee staff onboarding, training, and administrative activities in the offices of Principal Investigator, Dr. Stephen Freedland, and his associates at his urology and oncology research lab.
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Evaluating Regulatory Requirements: Responsible for assessing the regulatory compliance requirements for IT, including AML/BSA, Deposits, Lending, CRA/HMDA/Fair Lending, Financial Products, Privacy, and Safety and Soundness regulations.
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affairs job Title: regulatory affairs in Durham, NC
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