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Should have experience of independently authoring complete 510k submissions, Health Canada Medical Device license applications (Class II or above), EU MDR technical file dossier (Class II or above.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Master the contract plans, specs, and contracts/subcontracts. Manage client-related submittal software (Procore, E-Builder, Autodesk). Review the scope of work with the Project Superintendent.
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Job Description Global Property and Casualty Provider seeks an experienced Scrum Master to play a crucial role in the roll out and ongoing maintenance of the Guidewire InsuranceSuite to enhance the company’s core business operations.
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The OpportunityQuidelOrtho 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.
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Patient Mix: 11 bed unit with IMC/Tele; Hematology/oncology, chemo, autologous bone marrow transplant and CAR-T (Stem cell) overflow, bone marrow biopsy, new leukemia inductions, multiple transfusions, count recovery, and clinical trials.
$2,520 a weekExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Project management skills and experience are a plus, as are SCRUM Master or Product Owner certifications. A ServiceNow certification is highly desired (e.g., Certified System Administrator, Certified Implementation Specialist.
$68 an hourExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Allowing the new graduate nurse to gain clinical competency and achieve transition from student to professional practice. 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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The role will interface with multiple cross-functional teams including pharmacovigilance, quality, medical directors/leads, field medical team, commercial, regulatory, legal, and clinical development as well as external partners.
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May also perform general administrative assistance including but not limited to opening, closing and maintaining the office, clubhouse and amenities, maintaining office organization and file structure, logging and retrieving customer packages.
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Under the direct supervision of the PCMH Care Coordinator (PCC) or Site Manager and under a matrix system of supervision and guidance of the Director of Nursing, the Certified Medical Assistant (CMA) assists patients and their families in all aspects of their clinical interaction with their provider.
$19 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Comprehensive cancer center: onsite imaging, rehab, nutrition, genetic counselors, radiology, and surgical support, and clinical trials. Opportunity to participate in high-quality clinical trials.
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Participates in clinical activities (i.e. assists with patient flow/care, helps to optimize throughput of patients via Radiology Ambassador team. Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols.
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SAFe Scrum Master certification or Scrum Alliance CSM (certified Scrum Master). At least 6 years of experience as Scrum Master Facilitating ceremonies (Sprint Planning, Daily Stand up, demos and retrospective.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Develops, authors and executes study protocols and amendments by literature investigation, database searches and other existing/investigational products, liaising with key opinion leaders (KOLs), clinical trial investigators and internal scientific, pharmacology and regulatory teams.
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The candidate will be responsible in the purification of 50L to 1000L volumes engineering, clinical and commercial batches in a cGMP environment. RequirementsEducation:Requires a Bachelor or Master' degree in chemical, biological or biochemical sciences and a minimum of 8 - 12 years of related experience in the biopharmaceutical industry.
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clinical master file jobs Title: trial master in Somerset, NJ
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