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We are currently looking for an Operations Specialist to oversee the livestreams on TikTok. This would be a great opportunity for the right candidate to become an expert in live selling and kick off an amazing career in one of the fastest-growing commerce spaces.
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The Senior Risk Specialist is responsible for leading and/or participating in the most complex reviews and examinations that evaluate the effectiveness of risk management practices for large, globally systemic financial institutions under Federal Reserve supervisory authority.
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Bioinformatics NGS Data Analyst
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Additional specific qualifications in the area of clinical supply chain planning including APICS CPIM or CSCP, and related professional certifications. Reporting to the Head of Clinical Supply Chain, the Associate Director of Clinical Supply Planning will focus on managing and optimizing global supplies to ensure timely availability of clinical supplies for 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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As an AI Content Writer you will be responsible for reviewing machine and human generated demonstrations in order to generate preference data for training purposes.
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Strong knowledge of biomarker technologies and methodologies, including genomics, proteomics, imaging, and flow cytometry, as applied to clinical research. Senior Scientist, Clinical Biomarkers 142424 Posted: 01th April 2024 140000 USD - 180000 USD Boston , United States Permanent Job Title: Principal Scientist, Clinical Biomarker Company Overview: Join a dynamic and forward-thinking mid-sized biotech company dedicated to advancing breakthrough therapies and diagnostics in the field of life sciences.
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You will also be responsible for configuring, maintaining, and managing multiple CAD applications, and PDM/PLM systems. We are looking for a CAD Specialist to join our Engineering Services team within our Hardware organization.
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Deep understanding of drug development, study conduct processes, GCP and regulations related clinical data management as well as ICH guidelines, FDA/EU regulations. Responsible for managing the clinical trial data queries along with the planning and execution of medical coding and SAE reconciliation.
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The Clinical Trial Manager, Site Start-up will lead internal process improvements related to study start up activities to ensure clinical trials are executed with high quality standards in compliance with regulatory requirements, GCP, and company SOPs. This role is based in our Waltham, MA headquarters.
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Day Shift 7:30 am- 4 pm Requirements for the Medical Laboratory Technologist- Histocompatibility:Bachelors degree in biological or chemical science or medical technology or clinical laboratory scienceCertified Histocompatibility Specialist (CHS) certification required (ACHI)Minimum of three years of progressively responsible experience in a Histocompatibility (HLA) testing environment (at least 1-3 years in a lead/supervisory role is preferred.
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Imagine a future where you support our portfolio of renewable energy projects while building regulatory expertise in historic and cultural resource protection
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Responsible for external outreach with KOLs and key clinical trial sites to provide feedback on study feasibility and study start up activities. Clinical Trial Initiation Manager will deliver high quality and timely global study start-up.
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Drug Safety and Pharmacovigilance Support: Oversee safety and pharmacovigilance activities, ensuring data quality control and effective management of adverse events, including non-serious and serious events, adverse events of special interest, and signal detection across clinical laboratory, vital signs, and ECG data.
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Founded by an internationally recognized team of neurodegenerative biologists from Harvard Medical School and Harvard University, QurAlis is a clinical-stage biotechnology company advancing a pipeline with therapeutic candidates that target specific components of ALS and FTD pathology and defined patient populations based on both disease-causing genetic mutation(s) and clinical biomarkers.
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Title: clinical applications specialist in Somerville, MA
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