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Experience and familiarity with quantitative research and data is strongly preferred, including expertise in biostatistics, bioinformatics, computational biology, clinical imaging, machine learning, genetics, proteomics or data science.
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Tufts 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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Education: Associate’s degree in Medical Laboratory Technology, Clinical Laboratory Science, or a related field. Requirements Experience: Minimum of 1 year of experience in a clinical laboratory setting preferred.
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PepGen is looking for a highly motivated Associate Director or Director level Biomarker scientist who will contribute to the preclinical/clinical development to support and expand their current and future pipeline.
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The Research Scientist is responsible for designing, developing and validating clinical qPCR, RT-qPCR and ddPCR based molecular diagnostic assays and transfer of validated assays to the clinical laboratory.
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Research is supported by the National Heart, Lung, and Blood Institute, American Society of Nephrology and the BWH Khoury Innovation Fund. Under the supervision of the Principal Investigator and research staff, the Research Analyst Intern will conduct analyses with and develop pipelines for various types of omic data as well as clinical datasets from epidemiologic studies and clinical trials.
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Deep knowledge of immuno-oncology biology, biomarker strategies and application to clinical trials. Working with Research Unit biology leads and Precision Medicine Companion Diagnostic leads to ensure alignment of preclinical, clinical biomarker and CDx strategies.
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Dr. Zhang’s laboratory uses an interdisciplinary approach that integrates computational biology, cell and molecular biology, as well as physiology and biophysics to address fundamental questions and explore potential translational targets for a variety of kidney disorders, including acute kidney injury, chronic kidney disease, and graft dysfunction following kidney transplantation.
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Manages the DFCI Biosafety Communications Program by identifying topics relevant to investigators with biosafety protocols such as upcoming modifications to IRIS for human gene therapy clinical trials and iRIS-IBC for laboratory registrations and any regulatory and DFCI policy updates, training requirements, resources and guidance, and those requested by the Director of Biosafety.
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West Newton Healthcare is seeking a Clinical Manager Licensed Practical Nurse (LPN) Nurse Supervisor. Currently seeking an exceptional Clinical Manager Licensed Practical Nurse (LPN) Nurse Supervisor to join our team in our West Newton Healthcare facility.
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Responsibilities Include: Conducting all trial visits Completing all study-specific assessments (e.g. vital signs, EKG, blood collection) Processing all samples and shipping to Central Lab Maintaining study source Entering data into sponsor EDC and query resolution As the sole Senior Clinical Research Coordinator (SCRC) on-site, the chosen candidate must be adept at protocol comprehension and be capable of working autonomously.
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Provides ad-hoc programming support to Clinical Operations, Data Management, Statistical Programming, Biostatistics, Drug Safety, Clinical Science, Medical Writing and Drug Safety to ensure rapid access to clinical study data for data cleaning/validation, SAS listings review, TLF, dry runs, etc.
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Supervisory Responsibilities: With the exception of Licensed Independent Clinical Practitioners, the SVP of CHCs supervises clinical and non-clinical health center departments including but not limited to Nursing, Clinical Support, Dental, Pharmacy, WIC, Call Center, Practice Management, Referrals, Quality Improvement, Lab and Administrative Assistants.
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The company has approved medicines that treat the underlying causes of multiple chronic, life-shortening genetic diseases — cystic fibrosis, sickle cell disease and transfusion-dependent beta thalassemia — and continues to advance clinical and research programs in these diseases.
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Represent non–clinical development on project teams and interface with internal stakeholders in discovery and development, as well as interface with regulatory agencies. Lead toxicology and nonclinical development for Seaport's small molecule portfolio across preclinical and clinical development.
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clinical laboratory jobs Title: project director in Boston, MA
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