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A Clinical Research Coordinator I is asked to perform an increasing complexity of tasks to facilitate clinical trials at Virginia Mason, working with a variety of sponsors ranging from large pharma and biotech sponsors to small non-profit grant awards.
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We're a leader in staffing Clinical Development, Clinical Operations, Regulatory Affairs, Medical Affairs, HEOR, Market Access, and Sales & Marketing roles. TMAC's direct-hire service, formerly known as TMAC Direct, is an award-winning executive search firm that specializes in permanent placement services for the Pharmaceutical, Biotech, Diagnostics, Device, and Life Science Research industries.
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In coordination with the Associate Dean of Students, the AVPDOS oversees the establishment and training of hearing panels, assures the adjudication of student code of conduct violations, and coordinates the Division of Student Affairs response to student emergencies.
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A current Certificate of Clinical Competence issued by the American Speech/Language/Hearing Association (ASHA) and valid State of Michigan Speech-Language Pathologist license issued by the Michigan Department of Licensing and Regulatory Affairs, Bureau of Health Care Services for CCC-SLP, CF (In Process.
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The Stephens Family Clinical Research Institute at Carle Health would like to hire a Associate Research Scientist for the Carle Clinical Imaging Research Program (CCIRP.
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A minimum of 6 years' experience in pharmaceutical, medical, device, biotech, or clinical trial contract research industry, including minimum 2 years' experience in Quality Assurance and/or Regulatory Compliance/Affairs.
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Student data Management - Working closely with the Associate Dean of AA, works collaboratively with admissions, academic and student affairs and institutional effectiveness to manage student data for all CAHS academic programs.
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Conduct legal research and analysis on regulatory issues related to blockchain and cryptocurrency. As an Associate Attorney in our Web3 practice, you will work closely with senior attorneys and clients to navigate the complex legal landscape of blockchain technology, cryptocurrencies, decentralized finance (DeFi), and related fields.
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All who are selected to participate in CFR’s Blavatnik Internship Program and Robina Franklin Williams Internship Program receive training in the field of foreign policy and international affairs as well as skills training in writing, research, program planning and much more.
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The primary responsibility will be to interpret and report clinical cases in molecular diagnostics and assist the Division Director with assay design, feasibility studies, and clinical validation consistent with all regulatory guidelines (CAP, CLIA, FDA.
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Summary: The Sr. Psychologist serves as the Associate Director for NMSU Counseling & Psychological Services and is responsible for providing oversight for clinical services and related staff management and administrative duties.
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We research, develop, and commercialize innovative digital health products and solutions by bringing together the full capabilities of our team, including product strategy and management, clinical expertise, partnerships, UI/UX design, usability research, clinical research and validation, software development, AI / Gen AI, and regulatory.
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Participates in the coordination and completion of multidisciplinary efforts in regard to regulatory preparedness and completion of applications (e.g. Hospital Accreditation and Licensure, CMS Database Forms, ICM completion, measurement of success data, DPH/DOH or CMS corrective action plans, and clinical charter teams.
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The function maintains a critical linkage and partnership with internal stakeholders including GTI leadership, regional sales and marketing, global strategy & market development, market access, medical & clinical affairs, governmental affairs, innovation & development, operations, finance, global services, regulatory affairs, and quality.
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The Associate assists in maintaining contract records in compliance with institutional research sponsor policies and supports data entry into the OnCore clinical trial management system to document the status of all steps pertaining to budget and coverage analysis in the task management module.
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clinical research regulatory affairs associate jobs Company: Novo Nordisk A S in TX, Us
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