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The CRU Regulatory Affairs Office seeks a full-time Regulatory Affairs Veeva Quality Assurance Specialist to participate in the review and migration of Phase I-V clinical trial investigator site files to the Veeva SiteVault platform.
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The newly established Immune Health Initiative is hiring a full-time Regulatory Affairs Specialist or Senior Regulatory Affairs Specialist to assist with departmental IRB maintenance and submissions and to perform routine internal study monitoring for all observational clinical research studies.
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Collaborates with Student Affairs and Global Centers to support and improve student and exchange visitor services/initiatives. Masters in Public Administration, MBA, Masters in International Relations, Masters in Higher Education, Juris Doctor, or equivalent preferred.
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Communicate frequently with other Respiratory Sales Specialists across the country and cross-functional counterparts such as Marketing, Sales Ops, Market Access, Field Reimbursement, Training, and Medical Affairs to create alignment of business plan, focus on strategic drivers, and sharing best practices.
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This position reports to the provost/vice president for academic affairs. REPORTS TO: Vice President for Academic Affairs. The university is home to six professional performance venues, a production shop, costume shop, design studio, and lighting lab as well as countless studios, galleries, and multi-use spaces.
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Reports to: Vice President for Academic Affairs and Provost. The Dean of Academic Innovation is responsible for providing strategic leadership and vision to the Pottstown Campus and in service to Academic Affairs.
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The Quality Manager is also responsible for clinical privilege development and management of the TUHS Medical Staff Affairs Department, internal Credentialing Verification Organization (CVO) which oversees the credentialing of TUHS physicians and APPs working in non-licensed TUHS facilities.
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Reporting to the Regulatory Affairs Manager, the Regulatory Affairs Specialist will, with minimal supervision , prepare and process all regulatory documentation through the IRB, CTSRMC, FDA and all applicable regulatory review committees- including new submissions, continuing reviews, amendments, adverse events, and reportable events.
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The Director of Academic Affairs would have several direct reports and oversee several academic-facing functions, such as our Research Grant Administration Officer, our institutional Compliance Department/resources, and the Scientific Grant Writer.
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Cultivate strong client relationships, oversee project teams, and conduct comprehensive project reviews to ensure success. Manage procurement processes and enforce strict safety protocols throughout the project lifecycle.
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Title Temporary Part-time Athletics Facility Operations and Event Assistant Location Blackwood Campus Department Student Affairs Days and Hours 25 hours per week Requisition Number Job Description.
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Support coordination and implementation of global HTA strategies, including dossier development and submissions, in collaboration with Medical & Scientific Affairs and Market Access colleagues.
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Supports special projects or additional duties as determined by the Associate Dean for Academic Affairs and the Director of Regulatory and Master of Professional Nursing Program Qualifications BA/BS required; 2-3 years of work experience with progressive responsibility.
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Foster teamwork and collaboration amongst cross-functional partners to support the business: medical affairs, device support specialists, marketing, finance, reimbursement sales operations, and Learning & Development.
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Reporting to: Senior Director, CMC Regulatory Affairs, The Manager/Sr. Manager, Technical Writing - CMC (Chemistry, Manufacturing, and Controls) Regulatory Affairs plays a critical role in ensuring compliance with regulatory requirements pertaining to drug development and manufacturing processes.
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affairs job Title: regulatory affairs project manager Company: Gpac in Philadelphia, PA
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