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New York City (Hybrid On-Site): $149,000 - $149,000 for Data Science InternSan Francisco, California (Hybrid On-site): $158,000 - $158,000 for Data Science Intern. On any given day, you might:Evaluate open-source and internally-developed modeling and analytics tools using real business dataIntegrate internal data with external data sources and APIs to discover and implement actionable insightsDesign and craft data science models to communicate solutions to customers and company leadership We'd love to find someone who is.
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Our research aims to improve quality of life, well-being, symptom and pain management, and reduce caregiver burden:For example, a Clinical Research Coordinator to support a large multi-site clinical trial study that focuses on the comparison of care delivery models to support older adults with complex healthcare needs.
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What You'll Do: Review and audit assembled furniture for quality and value on-site at Wayfair warehouses in Taunton and Norton, MA.Confirm schema tags, imagery, and other product details are correct.
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Play a pivotal role in hotel sales efforts including calling on top ten accounts meeting clients hosting luncheons and receptions and meeting with on-site contacts on a daily weekly and monthly basis.
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With support from the CCBB Site Coordinator and BWH Center for Clinical Investigation, manage the coordination of umbilical cord blood donations for public banking and research, ensuring compliance with SOPs and regulatory standards for Tissue Manufacturing.
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The job: Provide customers with maintenance, repair, and installation assistance for CNC machine tools on-site or by telephone. Contribute to product development by assisting and training the end customer's Service Engineers on installing and maintaining newer product lines.
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Previous experience on a Site Leadership Team or R&D Leadership Team is strongly preferredHybrid-Eligible RolesIn this Hybrid-Eligible role, you can choose to be designated as: Hybrid: work remotely up to two days per week; or select On-Site: work five days per week on-site with ad hoc flexibility.
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Completely on-site in lab Description The ideal candidate should have immunoassays experience and a working knowledge of virology, molecular biology, and/or immunology. Job Title: Research Analyst Location: Cambridge, MA Duration: 12 months on Contract Top skills: Immunoassays experience and a working knowledge of virology, molecular biology, and/or immunology.
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Responsibilities: Technical Leadership: Lead by example, contributing hands-on expertise in Python, Airflow, Snowflake, and AWS to develop scalable and efficient solutions. Job Title: Hands-On Engineering Manager Location: Newton, MA About Us: My client is a rapidly growing eCommerce beverage distribution company that achieved $200 million in revenue last They are at the forefront of revolutionizing the beverage industry by providing exceptional service and innovative solutions.
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The Clinical Trial Manager, Site Start-up role plays a significant contribution to the clinical trial execution and ability to meet the corporate study goals for the Company clinical 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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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. 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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Develop a Site Initiation Management Plan and coordinate regulatory and ethics committee submissions and perform day to day management of the study start up activities for clinical studies. Clinical Trial Manager, Start Up Job Description; (Hybrid in office 3 days peer week) At Company, we are focused on developing best-in-class medicines for people living with autoimmune and rare diseases.
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Serves as a point of escalation for study teams and CROs for country and site activation issues. Reporting to the Director/Senior Director of Clinical Operations, the Clinical Trial Manager, Site Start-up is accountable for leading, directing and overseeing end-to-end start-up, site initiation and site activation in collaboration with key stakeholders across multiple complex studies in a fast-paced environment.
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Job Description; (Hybrid in office 3 days peer week)At Company, we are focused on developing best-in-class medicines for people living with autoimmune and rare diseases. Responsibilities (including, but not limited to):•Provides key data driven insights to study teams for study, country, and site feasibility along with start-up and enrollment forecasting.
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on site jobs Company: Gpac in Waltham, MA
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