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Perform biomarker data analyses including pharmacodynamic markers (cytokines, peripheral immune cell profiles, and tumor protein markers) and exploratory biomarkers (genomic and transcriptomic changes, deriving gene signatures) to support dose-finding, patient stratification, and understanding of MOA in the clinical trials.
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Summer Interns will have an opportunity to be part of high-performing project teams developing new manufacturing platforms to produce mRNA therapeutics and vaccines destined for clinical trials and commercial licensure.
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There is an exciting opportunity within the Precision Medicine Biomarker Program Management (BPM) group at AbbVie. The Precision Medicine group uses advanced methods to discover biomarkers for use in clinical trials.
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They will lead, plan, and execute study-level activities for 1 or more trials, and interact with Translational Scientists, Project Leadership, Safety, Regulatory, Data Management, Biostats, and Clinical Operations to drive Clinical Development strategy, design, execution, and interpretation of clinical trial data.
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Majoring in Electrical Engineering, Chemical Engineering, Electrical Engineering, Civil Engineering, AI/ Machine Learning, Computer Science, Data Science, Business Analytics, Statistics, Environmental Engineering, Construction Management, Project Management, Power Systems, Information Technology or a related field.
$33 an hourInternExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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MS/ME/PhD/PharmD, or equivalent with training in pharmacokinetics, pharmaceutical sciences, or related disciplines and 5+ years of drug development experience in Clinical Pharmacology translating candidates from preclinical through early clinical development.
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For employment as Clinical Social Worker, LCSW, at the BWH Department of Social Work: - Employment as a Clinical Social Worker, LCSW, is contingent upon passing the LICSW exam. Licensure: Require current Massachusetts Licensed Independent Clinical Social Worker (LICSW) or Licensed Clinical Social Worker (LCSW), or must obtain MA Licensed Clinical Social Worker (LCSW) within 4 months of hire date.
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We are seeking a Manager/Senior Manager in IRT Systems, who will be responsible for managing Clinical IRT Systems, forecast tools and services and will serve as an expert resource in supply for multiple global clinical trials and the Systems Analyst, collaborating with Clinical Operations, Information Technologies and Quality Systems in the selection, implementation, and maintenance of GMP/GCP systems.
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In this role, you will combine your expertise in modelling and simulation with cutting edge pharmacology (both clinical and pre-clinical) and bioengineering and provide scientific leadership in advancing novel therapies to the clinic with minimal non-clinical in vivo studies.
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Brookline's Health and Human Services Department is seeking a part-time Clinical Social Worker to provide mental health and substance use and at-risk behavior assessments, intervention, individual, group and family counseling along with education to youth referred through the schools, juvenile justice system, and other referral sources.
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Employment as a Clinical Social Worker, LCSW, is contingent upon passing the LICSW exam. The Clinical Social Worker is required to take the exam within two months of eligibility and will be allowed up to two attempts within a six-month period to successfully attain LICSW.
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Ensures all appropriate strategic CMC regulatory aspects for clinical trials, product release and stability are in place, to avoid clinical holds, and to ensure continuity of market supply.
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Data quality surveillance of CRF and external/non-CRF clinical trial data (e.g. Biosample Lab Data, Biomarker Data, Imaging) in collaboration with other Clinical Operations roles, Medical Monitors, Translational Medicine, Clinical Pharmacology, Biostatistics, and other internal and external stakeholders.
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Under the general supervision of the Clinical Manager and Clinical Supervisors, the Medical Laboratory Scientist Senior I (MLS Senior I) is responsible for the supervision of assigned workstations including Quality Control (QC) review, instrument maintenance and troubleshooting, training, competency assessment of staff, operations, and inventory management.
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In addition to its wholly owned clinical assets, Dragonfly has a deep pipeline of wholly owned preclinical candidates discovered using its proprietary platform, as well as productive collaborations with Merck, AbbVie, Gilead and Bristol Myers Squibb in a broad range of disease areas.
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