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Reach & Scale: The products and platforms this group builds and operates delight millions of consumers every minute of every day – from Disney and Hulu, to ABC News and Entertainment, to ESPN and ESPN, and much more.
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Works with the Sr. Manager patient safety and risk at BWH/BWFH and clinical leaders to prepare regular presentations to the Board Quality Committee, Care Improvement Council, Quality Assurance/Risk Committee, and other BWH/BWPO leadership and clinical groups, as needed.
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Lead toxicology and nonclinical development for Seaport's small molecule portfolio across preclinical and clinical development. The VP, Non–Clinical Development leads the development and execution of the toxicology profiling of Seaport's drug candidates, including risk assessment /mitigation, development of innovative toxicology strategies, and communication of plans throughout the organization to ensure cross–functional alignment.
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Bachelor of Science (BS) or Arts (BA) college degree or equivalent clinical degree i.e., Registered Cardiovascular Invasive Specialist (RCIS), Certified Cardiology Technician, Registered nurse (RN) or Nurse Practitioner (NP), Transcatheter Cardiovascular Surgical/Scrub technician, Physician Assistant (PA.
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The Process Improvement/Project Management Specialist, Remote for Beckman Coulter Diagnostics is responsible optimizing customer organizational performance by leading the implementation of cost savings projects that track directly back to the customers P&L. Also, enhancing the alignment and efficiency of business processes by ensuring continuous, sustained improvement across the enterprise through the implementation of Danaher Business System like tools and methodologies.
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Remain current on HNRCA fire and safety procedures, biosafety and radiation safety requirements, and MRU and HNRCA trainings related to best practices and safety procedures related to clinical research and protection of research participants.
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Deep understanding of drug development, study conduct processes, GCP and regulations related clinical data management as well as ICH guidelines, FDA/EU regulations. Responsible for managing the clinical trial data queries along with the planning and execution of medical coding and SAE reconciliation.
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The individual will coordinate and manage daily data management and vendor oversight activities for multiple clinical trials to support both the internal project team and the CROs. Reporting to the Senior Director, Clinical Data Management, the Associate Director, Clinical Data Management will define and lead the clinical data management strategy for the organization.
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Responsibilities LCSW or LICSW RequiredExciting and challenging opportunity as a dedicated ambulatory social worker providing clinical social work services to patients and their families at the Dana-Farber Cancer Institute’s Longwood Medical Center location.
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The MGH Cancer Center is seeking a Clinical Research Associate Manager to join their team. Develops and maintains database of all MGH GI oncology clinical research publications and grants, including collaborative publications.
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Crafting Brighter Futures for Families
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Experience working in an Operating Room, Electrophysiology (EP) Lab or Catheterization lab either through industry or clinical setting preferred, but not required. Conduct in-person meetings with surgeons and support staff to discuss AtriCure technology, training programs, clinical trials, and more.
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This growing, fast-paced startup company is looking for a Strategic Purchasing Specialist who will be responsible for assisting in the sourcing of critical material for capital projects, as well as the procurement, planning, and sourcing of material for our new production facility.
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The Clinical Trial Manager, Site Start-up will lead internal process improvements related to study start up activities to ensure clinical trials are executed with high quality standards in compliance with regulatory requirements, GCP, and company SOPs. This role is based in our Waltham, MA headquarters.
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Applicants will be expected to provide clinical, technical, and regulatory experience in general chemistry, clinical toxicology, immunology, blood gases, and mass spectrometry at BMC. Responsibilities will also include, but not be limited to, quality management initiatives, protocol development, verifications, and supporting the Director and administrative team to ensure compliance with the regulatory requirements of College of American Pathologists (CAP), The Joint Commission & CLIA.
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Title: clinical specialist Company: Friendship House Pa in Boston, MA
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