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Previous experience working in a matrixed environment to implement flow cytometry assay development and validation to support clinical trials. Project management skills to meet critical timelines associated with various activities necessary to support biomarker assessment of clinical samples.
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In this vital role you will design, develop and implement clinical biomarker assays employing innovative flow cytometry methods and techniques to support our drug development efforts. Flow Cytometry, Clinical Biomarkers - Principal Scientist.
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Sarah Cannon Research Institute (SCRI) is one of the worlds leading oncology research organizations conducting community-based clinical trials. It has conducted more than 750 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA today.
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Meets requirements of Clinical Trials Senior Chemotherapy Nurse 30% Abides by requirements in accordance with the Oncology Nursing Society’s Manual for Clinical Trials Nursing.
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The Clinical Research Supervisor reports to the Research Administrator, Clinical Trials Manager, Research Vice Chairs and works directly with Principal Investigators within the Department of Obstetrics, Gynecology and Women's Health on the execution of reproductive health research studies, focusing on protocol development and coordination, supervising research/study assistants, and data cleaning and monitoring.
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This Transplant Coordinator position provides primary clinical management and coordination of care for all post-transplant adult kidney, pancreas, and liver transplant patients. Our health network operates eastern Wisconsin's only academic medical center and adult Level I Trauma center engaged in thousands of clinical trials and studies.
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Utilizes professional clinical skills, education and/or experience in project planning and implementation of data collection for complex clinical/health research trials. Utilizes professional clinical skills/training for independent decision making for data collection/trial intervention(s)/evaluation.
$46,420 a yearPart-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Explore and develop new opportunities to drive the CGLC program, which includes coordinating with multiple NIH-funded centers of excellence and eventually working with the Clinical Trial Office (CTO) and collaborating with existing Columbia infrastructure for pre-clinical and clinical trials.
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Data Management : Oversee biomarker data transfer among clinical sites, assay vendors, and internal teams, ensuring relevant metadata is associated with samples. Scientific and Operational Leadership : Lead biomarker data collection in clinical trials and non-interventional studies, ensuring robust and reliable data.
$350,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Outside of the Platform, the RWE Oncology Lead will work with leaders from Biostatistics & Data Management, Global Regulatory Affairs, Clinical Pharmacology / Pharmacometrics, HEOR, Legal/Compliance, and others to achieve research and business objectives.
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Piper Companies is searching for an experienced Board-Certified Neurologist to join a clinical research site in Raleigh, NC as a part-time Principal Investigator to provide leadership and support for clinical development and execution of neurology clinical trials.
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Schedule/conduct in-service training for appropriate staff on assigned clinical trials, regularly updating the Clinical Trials Management System (CTMS) with patient information and key dates to support responsible financial management of clinical trials with Clinical Research Coordinators.
$126,720.23 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Responsibilities include supporting the daily operations of data security event management and partnering with the Office of General Counsel and Compliance to process data security and privacy breach events.
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Active partners include investigators at Yale University, Osher Center for Integrative Health jointly based at Brigham and Women's Hospital and Harvard Medical School, The University of Iowa College of Public Health, and RAND Co. The PCCR has excellent clinical research support, including a dedicated research clinic, exceptional clinical research professionals, and an Office of Data Management & Biostatistics.
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As R Shiny programmer you will design, develop, deploy, and optimize user-friendly interactive web applications for clinical data analysis and visualization. We are seeking a talented R Shiny programmer to facilitate interactive reports that translate clinical trial data into clinical insights.
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clinical trials data management jobs Title: operations Company: Merck
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