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Leading a cross functional team for a) the identification of new indications for Alexion therapeutics; b) the functional differentiation of Alexion targets from competitors; c) driving rigorous translational understanding of clinical trial data, d) drive key translational/BM hypothesis for treatment response or non-responsiveness e) lead efforts to drive translational research strategy for the different programs in nephrology TA.
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The Clinical Research Coordinator, Level 1 (CRC1) is a research professional who ensures oversight and compliance of both system-wide and local SHC clinical research activities.
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Our client is a leading pharmaceutical company seeking a Director, Insights and Analytics for two different brands (2 different people). Drive insights agenda: Scope, lead, and deliver cross-functional projects across core insights functions, including market research, forecasting support, competitive intelligence, brand analytics, and field analytics.
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Performs research and potentially clinical diagnostic molecular imaging testing to include general, cardiac, and PET studies along with the computer interactions associated with these studies, in addition to supporting our Theranostics program.
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Through research, education, clinical practice and community partnerships, we are committed to the mission of advancing health, providing each person the best care, in the right place, at the right time, every time.
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A PhD and/or MD degree with postdoctoral experience and a minimum of three years of research in renal biology and physiology, preferably in the pharmaceutical or biotechnology industry. Internal Job Title: Principal Scientist IIJob Location: Cambridge, MA onsiteAbout the role:We are seeking an innovative and dynamic scientist with broad expertise in nephrology to join a vibrant research team focused on finding new transformative therapies for people living with renal disease.
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MA, EMT, CNA or LNA certificate, or Associates Degree in Medical Assisting or a t least 5 months of direct patient care experience in a clinical or research setting, such as: experience working as a medical assistant (MA), a patient care technician (PCT) or a clinical nursing assistant (CNA); nursing or medical student with completion of one clinical rotation.
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The Dana-Farber/Boston Children’s Cancer and Blood Disorders Center has a faculty numbering more than 100, with exceptional research and clinical programs in non-malignant hematology, hematologic malignancies, solid tumors, and neuro-oncology.
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PhD or PharmD required, with strong experience (15+ years) in the pharmaceutical or biopharma industry with clinical development, and/or medical affairs experience. This Leader is accountable for the development of the global therapeutic area medical strategy and execution of individual programs for late-stage development and in-line breast cancer assets, translating cross functional and geographic needs, and clinical / health system stakeholder insights into actionable research and medical deliverables to support the lightspeed development of innovative cancer medicines that takes on the world's biggest cancers and reaches every last patient faster.
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Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in MA, NH, MI, VA, SC, FL, GA, AL, MO, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine.
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Oversee the development and testing of clinical databases and data cleaning procedures, utilizing Medidata Rave/Veeva, and enforce data integrity through comprehensive documentation and quality control.
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Job Description: The Mechanism of Cancer Resistance (MoCR) Thematic Research Center (TRC) is seeking a highly motivated Associate Scientist to support Discovery Biology research programs at our facility in Cambridge, MA. The ideal candidate will contribute to our discovery pipeline from the bench by taking responsibility for developing, optimizing, and troubleshooting cellular assays to characterize and advance Client molecules of interest.
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Responsible for ensuring development programs are operating in compliance with the EU/FDA regulatory requirements and in compliance with company standards. Thorough knowledge of FDA and EU cGMPs and pharmaceutical manufacturing and analytical requirements.
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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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We are recruiting a Research Assistant I to work with a talented team of PhD students and postdocs on exciting projects dissecting the roles of immune cells that live at the borders of the brain (the meninges, choroid plexus, brain perivascular space) in healthy brain development and neurological disorders.
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clinical research pharmaceutical company jobs Company: Qps Holdings in Boston, MA
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