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The CSS will support internally sourced studies and studies out-sourced to Clinical Research Organizations (CROs). Performs scheduled reconciliations of study Trial Master File (TMF) with clinical study lead guidance.
$43.61 - $62.5 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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These functions are to include (but not limited to): Medical Records, Credentialing, Admissions/Intake, Accounts Payable, Billing, Collections, Insurance Verification, Transaction, Posting, Clinical Logs and other duties as assigned.
$16 - $24 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Listing as PI (Principal Investigator) or Sub I (Sub-Investigator) on Gynecology Clinical Studies for Cosmetics, Personal care and possibly OTC products. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations.
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QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine.
$57,000 - $98,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Under the direction of a Registered Nurse (RN), the Licensed Practical Nurse delivers efficient and effective nursing care while achieving positive clinical outcomes and patient/family satisfaction.
$30 - $37 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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In collaboration with the senior management and sales management teams, plan product strategies based on input from customers and consumers through field sales and market research. This position works in close collaboration with cross functional groups to drive downstream marketing execution, product innovation with research and development, and flow-through processes with manufacturing.
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Analytical mindset with proficiency in market research, data analysis, and performance tracking. While primarily focused on self injector launch, this individual will also work on base product (vial and syringe) as needed including supporting performance management (both vial & syringe and self injector) as well as strategy and operations for the immunology portfolio.
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Licensure/Certifications: Applicant must have ASHA Certificate of Clinical Competence in Speech Language Pathology. Not accepting Clinical Fellowship applications at this time.” DescriptionMatheny Medical and Educational Center has a career opportunity available for a Temporary Part Time or Full Time Speech Language Pathologist.
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Physical TherapistKey information:Title: Physical TherapistLocation/work environment: In facilityReporting structure: Reporting to Director of RehabPowerback 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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Sampled enables clients to advance human health by leveraging active biological samples through preservation, immortalization and utilization in comprehensive multiomics research within the only leading-edge Global Integrated Analytical Biorepository.
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Created by the 2019 merger of Summit Medical Group and CityMD, our integrated group of providers and comprehensive resources deliver strong clinical outcomes and an excellent patient experience.
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You will lead, plan, and execute process development activities from protocol generation through data analysis and report closure for Clinical Trial Manufacturing readiness. Join our dynamic team as a Staff Scientist, where you will support and lead portions of the Component Qualification process, focusing on device components made from various materials such as plastics, rubber, and metal.
$42 - $48 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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. BS in a scientific discipline.
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Solid knowledge and understanding of complex medical and scientific subject matter as well as evolving regulatory policy and guidance pertaining to drug development and commercialization. Global Life Science Hub is seeking a Vice President, Regulatory Affairs who will be responsible for building and leading a Regulatory Affairs department.
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As the leading academic health system in New Jersey, we advance innovative strategies in high-quality patient care, education, and research to address both the clinical and social determinants of health.
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clinical research scientific affairs jobs Title: director Company: Regeneron Pharmaceuticals Inc in Bridgewater, NJ
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