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In this role, as the Laboratory Coordinator can expect to learn about the functioning of a clinical fertility laboratory and expand their laboratory skillset through training in clinical laboratory and foundational embryology tasks.
$75,000 - $103,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The scholar will join a machine learning group with unparalleled direct access to clinical resources, as well as Stanford’s world experts in artificial intelligence, biology, and medicine. This is a unique opportunity for a machine learning scientist to directly impact patients’ lives in a clinical setting.
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Under the general direction of the Vice President of Operations and clinical guidance from the Chief of Cardiology, the Practice Manager of Testing and Cardiology Programs assists in the planning, organizing, and directing of non-invasive cardiac testing services and programs.
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Build QSP models integrating biological, pharmacological, and physiological data to support drug development at all stages, from preclinical research to clinical trials and beyond, aiding in dose optimization, biomarker identification, safety and efficacy assessment, drug development decision-making, etc.
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The Senior Medical Science Liaison/Medical Science Liaison (Sr. MSL/MSL) is responsible for developing and maintaining professional relationships with internal and external stakeholders to provide rigorous medical and scientific support of clinical development and pipeline programs.
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Master’s Degree or PharmD/PhD with at least 2-3 years clinical trial/drug development experience. Coordinate the real time availability of quality clinical trial data, including safety, efficacy, pharmacokinetic and biomarker data, to provide consolidated information for dose escalation meetings and data reviews with investigators.
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Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it.
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Experience: Must have at least 24 months of clinical experience as a Licensed Vocational Nurse (LVN) within the past 36 months. Additionally, within 6 months of hire, must obtain a Certified Hyperbaric Technician (CHT) certification from the National Board of Diving and Hyperbaric Medical Technology (NBDHMT.
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What You'll Do As a member of Biogen’s Alzheimer’s team, your main role will be to effectively communicate complex clinical data, protocols, screening and treatment pathways, market access policies as well as patient support services information to hcps and key non-clinical stakeholders.
$146,900 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Current, valid, unsuspended Licensed Clinical Social Worker (LCSW); Licensed Clinical Psychologist (Ph. D.); Psychiatric Mental Health Nurse Practitioner (PMHNP); or Psychiatric Physician Assistant (PC) Licensure in the State of California is required.
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The new collaboration also aligns RWJBarnabas Health with Rutgers' education, research, and clinical activities, including those at the Rutgers Cancer Institute of New Jersey and Rutgers University Behavioral Health Care.
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Assistant or Associate Scientist who will be part of an established team working to evaluate clinical trial samples for immunological responses to vaccination by an internal vaccine candidate. experience in the performance of in vitro assays with clinical materials and the use of LIMS.
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You’re passionate about bringing home health and/or hospice care to your patient’s front door, and you pride yourself on your ability to think on your feet and deliver expert care outside of a clinical setting.
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Serve as the lead statistician on project teams, offer statistical insights into clinical development plans, review and contribute to study design and define study endpoints. Knowledge of FDA and EMA regulations, ICH guidelines, GCP and familiarity with standard clinical procedures.
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Strong understanding of clinical trial data structures, CDISC standards, and regulatory requirements (e.g., FDA, EMA, ICH) Play a pivotal role in leading statistical programming activities for multiple clinical trials, ensuring the timely and accurate delivery of analysis datasets, tables, listings, and figures.
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clinical job Company: Healthcare Connections in New York, NY
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