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Support IRT Co-Chairs as necessary and transition commodities into the team as launch progresses into saleable builds. Support IRT Co-Chairs as necessary and transition commodities into the team as launch progresses into saleable builds.
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To provide exceptional customer service while facilitating the successful execution of custom IRT software development projects. Minimum of 3 years’ experience in IRT. Project or Product Management-related certification (PMP, CAPM, PgMP, etc.
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Background in selling eConsent, IRT, eCOA and Connected Devices. Background in selling eConsent, IRT, eCOA and Connected Devices. Must demonstrate a sustained (3 + years) and successful track record selling professional services to Pharmaceutical, Biotech, Medical Device, and/or Clinical Research Organizations.
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Contribute to the design and implementation of cutting-edge Interactive Response Technology (IRT) systems for CTM management. Contribute to the design and implementation of cutting-edge Interactive Response Technology (IRT) systems for CTM management.
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Experience programming with clinical data within pharmaceutical and/or biotechnology companies, clinical IRT/eCOA systems, or EDC. Experience with any data analysis package such as SPSS, SAS, R, or MATLAB.
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Develop IRT and participate in User Acceptance Testing. Experience with IRT system and implementation. Maintain traceable documentation within TMF and other electronic document systems created from multiple GxP activities e.g., labels, production batch records, temperature excursions, QP releases, vendor minutes, AoR, and expiry related MTFs.
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0 to 1 years of experience in IRT or related field preferred. Suvoda is a global clinical trial technology company shaping digital experiences that enable clinical trial sponsor and site professionals to take full command over the inherent logistical complexity behind mission-critical and time-sensitive patient interactions in life-sustaining studies for therapeutic areas such as oncology, central nervous system, and rare disease.
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Key Responsibilities: Collaborate with internal and external Customers and Service Providers, including but not limited to Clinical Research and Development, Global Study Management and Monitoring (GSMM), Project Management, BMS Affiliates, Medical Affairs (MA), Regulatory, CMC, QA, Packaging Vendors, CROs, IRT Organizations, and Global Clinical Supply Chain Functional Operations to ensure all needs are met.
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Strong knowledge of Forecasting and Planning and proficient knowledge of related areas, i.e. Manufacturing, Packaging & Labelling, IRT, Logistics, Quality, Stability, etc. Proficient/Strong knowledge of IRT and CTMS systems.
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Boeing’s Ethics organization, part of Law and Global Compliance, is seeking Mid-Level Ethics & Compliance Specialists to support the Issue Review Team (IRT) within the Risk Reporting Organization located in Renton, WA; Seattle, WA; Everett, WA; Auburn, WA; Mesa, AZ; Charleston, SC; San Antonio, TX; Seal Beach, CA; Arlington, VA; St. Louis, MO, Hazelwood, MO; or Ridley Park, PA.
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Possess clinical supplies experience/knowledge in forecasting, demand / supply planning, IRT systems, inventory management, clinical labeling and distribution including cold chain, import/export, and reverse logistics.
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Collaborate with Global Clinical Supply Chain functions and external Vendors on the package design and label development for investigational product to meet all protocol and regulatory requirements. Proficient knowledge of import / export requirements.
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Manage work through tools such as NIH incident response (IRT) portal, Splunk, ServiceNow, Jira, Confluence etc. Experience in Vulnerability management and threat management tools such as Tenable Nessus, Netsparker, McAfee suite, Palo Alto, Amazon inspector and Cloud Watch etc.
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Work with IRT team on ticket triaging. Supporting the desktop systems for AAA Video Game Development Studio. Support AAA Video Game Devkit Infrastructure. Work with IRT team on ticket triaging.
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Supports design and set-up of IRT system. 3 plus years of prior experience in a pharmaceutical, biotech and clinical supply logistics environment preferred. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your familys well-being.
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