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The Protocol Data Abstractor (PDA) Team Lead is responsible for managing the team of protocol data abstractors responsible for abstracting protocol content (e.g., lead organization, participating sites, study status information, IRB, funding) with new trials and amendments, performing data updates, addressing user inquiry requests, associated with clinical trials reporting.
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The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.
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Summary Cartesian Therapeutics is seeking a Translational Research Scientist/Senior Scientist with extensive experience in clinical biospecimen analysis to join our team and support translational research related to Cartesians early- to late-stage Clinical Trials.
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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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Similar searchable job titles Clinical Quality Manager Health Information Management Supervisor Quality Improvement Coordinator Clinical Data Quality Analyst Healthcare Compliance Officer Keywords Health Information Management Clinical Quality Reporting Data Migration Regulatory Compliance Quality Improvement Legal Disclaimer: Cherokee Federal is an equal opportunity employer.
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For this role we are looking for an outstanding bioinformatician to enable translational science via integration of large-scale omics, clinical data, real world evidence and literature data to deliver precision medicine within our pipeline.
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Must have experience with WHO and FDA regulatory authorities as it pertains to the conduction of human clinical trials. Previous experience working with human patient enrolled in clinical trials Background in medicine, malaria vaccines, and malaria clinical trial conduct.
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As an Associate Scientist/Scientist within our Early-Stage Formulation Sciences team, you will independently design and develop formulation and drug product presentation for Phase 1 through pivotal clinical trials of Antibody-Drug Conjugates, novel biotherapeutic molecules, other high potent modalities (OEB4+) and monoclonal antibodies.
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Collaborative Members have access to a variety of services, customizable to their specific needs such as Direct Connect patient concierge, virtual consults and second opinions, research and clinical trials access, network case conferences, physician trainings, observerships, Learning at Dana-Farber, virtual lectures and symposia, nursing support and education, program development assistance, and business strategy assistance.
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We are hiring a Senior Statistical Analyst to leverage cutting-edge data science tools and methodologies on real-world clinical data for scientific research in precision medicine.
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Possession of Bachelor’s degree in a field related to biomedical research, clinical trials, health from an accredited college/university according to the Council for Higher Education Accreditation (CHEA) or four (4) years relevant experience in lieu of degree.
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Experience with data analysis and visualization tools such as Excel, Tableau, Palantir. This includes the design and analysis of high throughput studies using various types of "-omics" technologies such as array- and sequence-based genome-wide association studies, studies of tumor characteristics using integrated genomic data analysis, and molecular epidemiologic studies based on novel assays focused on the metabolome and microbiome.
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The ABA therapist / Registered Behavior Technician collects and records data to monitor the progress of a treatment plan and works in collaboration with the clinical supervisor to update the treatment plan as necessary.
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At least 2 years of prior experience acting as a lead data manager in oncology clinical trials. Associate’s degree in the health sciences disciplines or related field of study and a minimum of 8 years of experience in the data management of clinical trials.
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Well-versed in multiple disciplines, including the broad application of information technology; interpretation of information from a wide variety of sources including biological sequences and molecules; potential research uses of electronic health records (EHR); and issues related to clinical studies, clinical trials, and rare diseases.
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clinical trials data jobs Title: operations Company: Boston Pharmaceuticals in Olney, MD
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