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Epsilon is a global advertising and marketing technology company positioned at the center of Publicis Groupe. As an Epsilon Client Lead, you will be at the forefront of driving defining a new engagement model and driving growth for Telecom Client.
Full-timeRemoteExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Provide Technology Support in ERP Fusion (Finance & SCM), ADW, BICC, OIC, SOACS and work with other tech leads and developers to provide technical direction. Overall Technical Solution Architect/Lead for Finance and SCM modules in cloud (SaaS and PaaS.
Full-timeRemoteExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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Our goal is to lead the industry's transition to a modern, technology-driven firm, that creates raving fans out of our people, clients, and partners. Looking for a Senior Tax Associate who is adaptable to new processes, technology, and services.
$90,000 - $110,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Rapiscan Systems is an industry leader in detection technology, providing cargo and vehicle inspection systems and services for ports, borders, military, high-threat facilities, and checkpoints to help customers combat terrorism, drug smuggling, illegal immigration, and trade fraud.
RemoteExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Lead Mechanical Engineer PE - Competitive Salary, Bonus, Benefits, Work/Life Balance. For nearly 60 years, we have been devoted to fulfilling our clients M.E.P. Engineering needs, providing architectural lighting & mechanical systems design, building commissioning services, technology systems design, life support systems engineering, and fire protection engineering.
$90,000 - $125,000 a yearRemoteExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Lead account-based marketing strategy, drive technology deployment & adoption including partner solutions. Support account-based marketing strategy to drive technology proliferation campaigns including adoption and deployment.
Full-timeRemoteExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Cognizant Technology Solutions is looking for “Oracle Cloud HCM Lead “ to join in our team of IT professionals in a permanent role. We have an immediate need for a highly skilled Functional Lead with expertise in at least two full cycle Oracle Cloud HCM rollouts.
$142,300 - $183,800 a yearFull-timeRemoteExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Lead a portfolio of diverse technology projects and a team of developers with deep experience in distributed microservices, and full stack systems to create solutions that help meet regulatory needs for the company.
$234,700 a yearFull-timeRemoteExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Remote Project Lead needs 2+ years' experience Remote Project Lead requires: •Experience in working within complex software including Microsoft Excel and Outlook is required.
Full-timeRemoteExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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In addition they will, under the direction of the OE Lead and in partnership with HR Technology, create a set of standard reporting and analytics outputs to enable and support HR Business Partners and the HRLT.
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Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating compelling submissions that meet rigorous regulatory standards.
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Substantial clinical study protocol experience, as lead author, required. Experience being a project lead, or managing a project team. Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias.
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MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.
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Write and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.
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Not required, but experience with orphan drug designations and PSP/PIPs a plus. The ideal candidate would hold a Bachelors, Masters, or Ph. D. in scientific, medical, clinical discipline. Candidate must be an expert in MS Word, Excel, PowerPoint, and related word processing tools.
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