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Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. OverviewThe Research Nurse in collaboration with the physician, is responsible for the implementation and evaluation of clinical research in their specific program/area.
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Health and safety experience in the academic, research, or healthcare industry. Have the benefits of working within a large research university and academic medical center, which includes generous medical, dental, retirement, and tuition remission benefits.
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SUPERVISORY RESPONSIBILITY (if applicable): A Clinical Research Coordinator I does not have any supervisory responsibility. A Clinical Research Coordinator II may assist with the training and orientation of new staff members.
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In addition, the ideal applicant should have a strong programming background (e.g. Python, R, SQL, MATLAB) and the drive and enthusiasm to learn about clinical neuroscience by assisting in state-of-the art patient-centered research.
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This position reports to the Principal Investigator and the Pre-Clinical Surgeon of the Cardiovascular surgical and interventional research laboratory within the MCRI and requires surgical and anesthesia proficiency in a variety of laboratory animal species and animal models.
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The Rare Disease & Neurology (RD&N) Research Unit is seeking a talented and dedicated Sr. Associate Scientist to advance research for drug discovery and development programs. Senior Associate Scientist, Rare Disease Research Full-time.
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Research and Development Associate III. Contribute to research efforts on specific projects involving novel BBB targets and other modalities. Expertise with in vivo procedures, including injections (IV, SC, IP), blood collection and necropsy/tissue collection (brain, spinal cord, muscle and other tissues.
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The Investment Research Associate is a three-year rotational program in which a successful candidate will work across multiple investment teams at GMO. The Investment Research Associate role is a unique opportunity to work with quantitative and fundamental investors across a variety of asset classes including equities, fixed income, alternatives and asset allocation.
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OverviewTufts University School of Dental Medicine seeks a Research Assistant for an active basic science laboratory whose research focuses on translational studies on tissue engineering and regeneration, association of dental diseases with systemic diseases including diabetes, osteoarthritis and Alzheimer’s disease and cancer.
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Informational links EnvironmentThe Mike Toth Head and Neck Cancer Center is in the Simches Research Center at Mass General Hospital, in the Historic Beacon Hill Neighborhood of Boston. Our lab is housed within the Simches Research Center at Mass General Hospital and is affiliated with Mass Eye and Ear, Mass General, Harvard Medical School, and the Broad Institute of MIT. ApplicationApplicants should submit a resume and cover letter.
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We're looking for someone exceptional to join our growing team as a Principal Scientist in the Preclinical Research group. Collaborate with research and process scientists to execute translational and preclinical safety studies using Kelonia's novel LVV gene delivery technology.
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Duration: 6 months contract with possible extensionTo be considered for an interview, please make sure your application is full in line with the job specs as found below.
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The goal of the program is to facilitate collections-based research using resources at the HUH which include more than five million specimens of algae, bryophytes, fungi, and vascular plants with complementary Libraries and Archives.
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The Associate Director, Global Real-World Evidence & Health Outcomes Research Scientist will be accountable for engaging closely with medical and matrix stakeholders and partner effectively in data generation plan (DGP) planning, design, execution, translation and dissemination at the study level for the asset.
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Role OverviewThe Human Research Compliance Specialist (compliance auditor) provides education and support to researchers and is responsible for performing audits of IRB-approved clinical research protocols across our institutions to ensure compliance with FDA, OHRP and other state and government regulations, Good Clinical Practice (GCP) guidelines, as well as with our organization's clinical research policies.
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Title: research Company: Aclu Of Louisiana in Waltham, MA
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