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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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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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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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Oversee the informed consent process and translation of study required documents and participate in the development of study start up plans. The Clinical Trial Manager, Site Start-up will serve as an expert in study start-up practices by initiating efficient start-up activities and removing obstacles for study teams.
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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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Screen Rant is the #1 entertainment website on the web and publishes up-to-the-minute news on blockbuster movies, TV, video games, and comic books. Note that this role does not involve video production, video editing, screenwriting, or writing reviews.
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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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Responsibilities:Lead the scale-up of lab processes to pilot and production scales, focusing on improving metal recovery and reducing costs and environmental impact. Executing manufacturing scale-up and verification batches efficiently from bench scale to commercial production environments.
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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. Mass General Brigham is seeking a Registered Nurse (RN) OR - Operating Room for a nursing job in Belmont, Massachusetts.
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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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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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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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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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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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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 Title: nursing student in Woburn, MA
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