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As a Senior Application and Discovery Scientist, you will join the product management team for our AI, Cheminformatics, and automation drug discovery products. PhD (or MS) in computational chemistry, medicinal chemistry, cheminformatics, or a related field.
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Current, active, and unencumbered MA State License as a Licensed Independent Clinical Social Worker (LICSW), Licensed Mental Health Counselor (LMHC) or Licensed Marriage and Family Therapist (LMFT.
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The Clinical Specialist will work with the Regional Sales Director and Territory Manager within a defined geographic area to meet existing and potential customers (e.g., physicians, physician office groups at hospitals) to identify their clinical needs, goals, and constraints related to patient care and to discuss and demonstrate how the company's interventional portfolio can help them achieve their goals and meet patient/customer needs.
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Depending on the level of experience and expertise, this role includes the opportunity to lead a cross-functional CMC team consisting of Drug Substance Development (SMPD), Analytical Development, Drug Product Development, and adjacent functions (such as QC, QA, CMC regulatory affairs, clinical supply chain) with full accountability for the CMC strategy and its successful execution.
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At TREEFROG US site, this Senior Scientist will lead a team of stem cell biologists to support the pluripotent stem cell (PSC) expansion and differentiation efforts in the C-Stem capsule technology.
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Creative, flexible scientist that can thrive in change and interact with colleagues from multiple scientific disciplines. Technical proficiency in standard molecular characterization methods such as flow cytometry, immunocytochemistry, RNA analysis (Taqman, scRNAseq, etc), and standard plate-based assays.
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As part of the Clinical Appeal process, the Clinical Appeals and Grievance Coordinator (RN) collaborates with members of the Appeal and Grievance team, pharmacy team, and medical director teams to resolve all types of clinical issues across the clinical/pharmacy appeal landscape.
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Manages the DFCI Biosafety Communications Program by identifying topics relevant to investigators with biosafety protocols such as upcoming modifications to IRIS for human gene therapy clinical trials and iRIS-IBC for laboratory registrations and any regulatory and DFCI policy updates, training requirements, resources and guidance, and those requested by the Director of Biosafety.
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Perform evaluation and selection of adequate technologies for establishment of clinical biomarker assays that meet clinical laboratory standards and regulatory requirements. The candidate will provide direction to the Clinical Pathology efforts by serving as a Physician Scientist in Pathology who has strong knowledge in current clinical practice in the Oncology, Gastrointestinal, Hepatobiliary, Dermatology, or other related field.
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Primarily responsible for instructional preparation and teaching of nursing courses offered at the associate degree nursing level in the classroom, clinical and laboratory settings. Demonstrate ability to plan, organize, implement and evaluate instructional materials in assigned areas of classroom, nursing laboratory and clinical teaching.
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In the Clinical Research Center (CRC), the Administrative Coordinator is responsible for providing administrative support to the Senior Investigator of Clinical, Behavioral & Outcomes Research, the CRC Nurse Manager and Manager of Administrative Services.
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O working with analytical laboratories analysing research and clinical samples as part of laboratory routine work. · Manage regulatory compliance of diagnostic development and associated bioanalytical laboratory operations, to support development activities, with good laboratory practices (GLP), OECD regulations, FDA, EMA, PMDA and other relevant global bioanalytical and immunogenicity guidance documents.
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As an Application Scientist, you will be part of our marketing and sales team in Boston. Zurich Instruments is a technology leader in advanced test and measurement instruments and a pioneer in quantum computing control systems.
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Experience in rare disease, pediatric, diabetes or kidney and/or complex clinical trials highly preferred. Independently manage interactions with clinical monitors, data management, safety, regulatory, pharmaceutical science, QA team members etc., both internally and externally including our CRO Partners, to ensure ongoing performance alignment.
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The Senior Biosafety Program Coordinator works in the Research Laboratory Support Office (RLSO). Providing general research compliance support and oversight of laboratory research. Developing, writing, implementing and maintaining standard operating procedures for research laboratory operations.
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clinical laboratory scientist jobs Title: technologist in Boston, Dearborn-heights, Michigan
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