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RRT Contract Details: - $1,818 - $2,011 per week - 13-week contract with possibility of extension - NOC shifts available - Duties will include but are not limited to respiratory care services to individual patients and their families by the application of the clinical process in assessing, care planning, implementing, documenting, and evaluating the care given.
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Lead the RFI/RFP, negotiation, drafting and execution of contracts for nonclinical and clinical lab and data services, including master services agreements, work orders, consultancy agreements, termination agreements, etc.
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RN Branch Director, RN Branch Manager, Hospice Branch Director, Executive Director, RN Executive Director, RN Administrator, Hospice Administrator, Hospice Executive Director, Hospice Branch Director, Director of Operations, DON, Director of Nursing, Director of Clinical Operations, Home health administrator, Home health director.
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As a Clinical Manager, you may advance your career into an Area Team Lead or Director of Operations role. Training and advancement: You will enter our Clinical Leadership Program that creates and supports a culture of continuous learning for our managers.
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The Project Manager (PM) leads the coordination of projects, focused on clinical process development, tech transfer and GMP manufacturing of cell and gene based therapies. The Project Manager (PM) leads the coordination of projects, focused on clinical process development, tech transfer and GMP manufacturing of cell and gene based therapies.
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Will consider strong Clinical Fellowship Year (CFY) candidate for Long Term Substitute (LTS) positions in the Related Services program. Master’s Degree in Speech-Language Pathology Pennsylvania Department of Education Certificate in Speech-Language Impaired PK-12 is required Certificate of Clinical Competence in Speech-Language Pathology (CCC-SLP) is required.
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Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
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Critical aspect of the role includes defining an agile quality and compliance strategy that supports Digital Data unit in their effort to establish a standardized, resilient, and sustainable data pipeline - including data sources, data quality, data governance, data management and master data management.
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No Relocation Assistance Offered# 159791 - Piscataway, New Jersey, United States Our company invites applications for the Sr. Research Scientist/Principal Scientist position, Dermal Clinical Research, Personal Care/Skin Health based in our Piscataway, New Jersey location.
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If needed, gather additional clinical and or coding information, as necessary, in order to obtain prior authorization. Collaborates with designated clinical contacts regarding orders that require escalation to peer-to-peer review.
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Set-up, organize, and maintain clinical study documentation (e.g. Trial Master File documents, clinical study site documents, email correspondence, training materials, etc.
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Powerback is proud to offer a comprehensive and unique benefits package for those candidates that are qualified, including health insurance benefits, 401k, paid time off, clinical support network, online CEUs, on-demand pay, Visa or Green Card sponsorship, and more.
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The Candidate: Bachelor of Science in Analytical Chemistry/Pharmaceutics with equivalent industry experience Master of Science in Analytical Chemistry/Pharmaceutics preferred or more years of applicable industry experience in support of pharmaceutical product development Expertise in Instrumentation techniques: HPLC, GC, FTIR, UV, KF, and other wet chemistry testing.
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Vitalief, a fast-growing, “best of breed” Research and Clinical Trial Solutions Company, is committed to identifying talented and passionate clinical research professionals to join our exceptional team and support our clients in planning and executing successful clinical trials.
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Must have Bioanalytical experience so they can help lab troubleshoot issues when applicable, Outsourcing experience preferred but the major focus/must haves should be at least years (with masters or higher degree) or years (with bachelors degree) bioanalytical experience, regulated experience, experience supporting clinical studies, biomarker ops or analysis.
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clinical trials trial master file jobs Title: trial master file in Somerset, NJ
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