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Collaborate with research, clinical, and bioinformatics scientists to execute projects that translate scientific and clinical questions into analytical workflows, and exercise skill in delivering accurate data processing, quality control, and statistical analysis.
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The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. The Clinical Research Coordinator will work within the Lymphoma and Immune Effector Cell clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator.
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Top biopharma sponsors, clinical research organizations, healthcare providers and institutions rely on ConcertAI’s evidence-generation and digital transformation capabilities to advance precision medicine and medical innovation.
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Serve as the key development representative both internal- and external-facing stakeholders [e.g., Clinical Research Organization (CRO), Key Opinion Leader (KOL), Data and Safety Monitoring Boards (DSMBs), the Advisory Committee on Immunization Practices (ACIP), etc.
$184,000 - $269,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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About the Role A Senior Clinical Data Manager (SrCDM) has keen attention to detail and is responsible for leading and supporting the start-up and execution of several trials with a CRO or in-house to ensure data quality and integrity.
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The firm focuses on the translational phase of medicine to generate data that can support full clinical development, and eventual market launch, to reach patients in need. Experience designing, executing, and managing in vivo and in vitro studies with strong data analysis skills and proficiency presenting data.
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Collects & organizes patient data Maintains records and databases Uses software programs to generate graphs and reports Assists with recruiting patients for clinical trials Obtains patient study data from medical records, physicians, etc.
$33,000 - $47,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Data Coordinator works within the clinical research program and supports the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DF/HCC Clinical Trials Office and/or Partners HealthCare Institutional Review Board (IRB.
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Required Experience: Degree in epidemiology, biostatistics, data science, clinical informatics, public health, or related fields. We are seeking a highly motivated and capable Data Scientist to support Tempus NEXT, an AI-enabled care pathway intelligence platform that applies technology, data, and AI to enable precision medicine, empowering providers to tailor the next step in a patient’s care journey and foster value based care within health systems.
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Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best-in-class medicines to patients around the world.
$88,300 - $147,100 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Strong knowledge of statistical software packages; previous experience in data mining, demonstrated experience / expertise in problem solving Extensive understanding of relational databases and ability to effectively utilize statistical software – SAS, Stata, R and Python.
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Performs general laboratory animal work including: sterile technique, megakaryocyte isolation, bone marrow isolation, and tissue collection/preparation. Specific Area of Research: Hematopoiesis, Microparticles, Megakaryocyte/Platelet Cell BiologyThis Research Assistant I will be responsible for: Isolate primary megakaryocytes and platelets needed for weekly experiments.
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MS in life sciences with a focus on in silico approaches (e.g. Bioinformatics, Computational Biology, Genomics, Computer Science, Physics, Statistics, Data Science or similar). Design and build bioinformatics workflows for the analysis of proteomics and other omics data (e.g. transcriptomics and metabolomics) to lead biology and disease relevant insight generation from internal data and external databases.
$92,000 - $157,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Job Title: Research Associate III OBJECTIVES: Develop methods for quantitation and characterization of viral vaccines and immune responses, including participation in project planning, execution, data analysis, and interpretation.
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Full stack software engineering experience, with proven experience in data visualization modules or frameworks like Python Dash and R Shiny. We are looking for a Senior Quantitative Developer that will be a part of a dynamic and fast-paced development team within Quantitative Research and Investment Technology supporting Fidelity Asset Management Solutions (FAMS) researchers and analysts.
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clinical research data collection trials jobs Title: specialist in Boston, MA
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