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PRINCIPAL DUTIES AND RESPONSIBILITIES: Study Start-Up·Oversight of the clinical trials start-up process from receipt of proposal materials, protocol development, IRB submissions, through site(s) activation.
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Coordinating with the Parks Department during inclement weather to ensure optimum use of the skating rink and providing up-to-date closure details to the public. Coordinating with the Parks Department during inclement weather to ensure optimum use of the skating rink and providing up-to-date closure details to the public.
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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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We focus on ground-up heavy civil, civil, and large commercial projects. A bit about us:Heavy Civil Superintendent opening with one of the world's largest and most well-funded development teams.
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To join our studio in Boston to work on Project Orion, the follow-up to Cyberpunk 2077 and the next major video game in the Cyberpunk franchise. Dog-friendly office — dog owner? Knowledge of industry-standard tools like Houdini, Blender, Substance Designer.
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Assists and collaborates with the Circulating nurse and Surgical Technologist to set up for surgical procedures with proper instrumentation, equipment and supplies. The O.R. Surgical Aide is responsible for maintaining inventory levels of specified stock items in the Operating Room, and the preparation of stretchers and oxygen tanks to see that both are ready and available when needed for patient transport.
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By seamlessly integrating semiconductors with conventional microplates, Pixel unlocks multi-modal electrical, electrochemical, and electrophysiological capabilities, delivering an unprecedented scope of data collection and scale-up for cell biology research, drug development, and pharmaceutical manufacturing applications.
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Your role : You will serve as the primary pharmacovigilance lead on study teams and liaise with cross functional team members, as well as external vendors and services providers; performing drug safety study start-up, maintenance, and close-out activities.
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As the CPQP lead, the incumbent is expected to provide subject matter expertise and program level functional leadership on issues related to clinical pharmacology, pharmacokinetics and pharmacodynamics (PK/PD), cell therapies, and genetic medicines from the pre-clinical stage up to the registration stage.
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Continue to care for our members beyond the lab room by answering patient messages, following up on lab cases and assisting our providers and virtual medical team with clerical duties such as, but not limited to biometric screening forms, medical record and consult review, billing inquiries, and DOH reporting.
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Oversee CROs to produce recombinant proteins and antibodies for in vitro screening and scale-up for in vivo studies, manage in-house inventory, help build LIMS and lab as company grows. Knowledge of techniques and instrumentation related to protein characterization and analytics (SPR/BLI binding, LC/MS, peptide mapping, PTM characterization, HPLC, DSC, DLS, etc.
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Keep up with current developments in methods, standards, and requirements for training in animal research and current laws, regulations, and policies governing animal research, teaching, and testing.
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Up to 10% domestic and international travel required; Up to 20% remote work allowed. Description Takeda Development Center Americas, Inc. is seeking an Engineer IV in Lexington, MA with the following requirements: Master’s degree in Bioengineer, Biology, Chemical Engineer, Chemistry or related field plus 3 years of related experience.
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CD PROJEKT RED is looking for an Expert Character Artist to join our studio in Boston to work on Project Orion, the follow-up to Cyberpunk 2077 and the next major video game in the Cyberpunk franchise.
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Proven experience with all phases of automation projects including conceptual, basis of design, implementation, testing, start-up and commissioning of Process Control System (PCS), SCADA, and DCS in the Life Science industry.
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up job in Malden, MA
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