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Bachelor's degree from an accredited college or university is preferred; certifications in ServiceNow Administrator, Application Developer, Implementation Specialist (CSA, CAD, CIS), Implementation Specialist (one or more focuses in ServiceNow) are preferred; Industry Certifications including SAFe Product Owner, SAFe Implementer, SAFe Agilist, and Scrum Master are also preferred.
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The Building People's Market Offerings and Business Lines include: Real Estate & Workplace Facilities Management & Maintenance Engineering & Construction Management Energy & Environmental Technology Integration Sustainability & Smart Buildings Human Capital Mission Support Can be 100% Remote The Building People, LLC, has a position open for a full-time Realty Specialist to provide realty support services to the Bureau of Alcohol, Tobacco, Firearms and Explosives.
Full-timeRemoteExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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We are a gambling technology company launching a new service and looking for individuals to join a focus group in an ongoing part-time capacity. This position is open to any person seeking short-term, work at home, part-time or a full-time job.
RemoteExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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National Support Specialist, GE - NM/PET-CT/SPECT (Remote/Travel: US) Demonstrated skills and experience with IT networking technology. We are a health technology company.
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Work alongside the business units, MES project teams, technology teams, and subject matter experts to gain an understanding of the project and related requirements to develop an appropriate APD.
$50 - $55 an hourRemoteExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Work in an office/home office and/or remote setting, as well as in a hospital/healthcare environment; adhere to requirements. You have an Associate Degree in electronics or equivalent combination of education and experience; BSEE/BSEET/BSME/BSMET preferred.
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The Medicare Claims Resolution Specialist is primarily responsible for working claims after they’ve been submitted to Medicare. Digitech is a leading provider of advanced billing and technology services to the EMS transport industry.
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The BTS Communications Specialist position will be responsible for working with BTS leads to create/develop the communications written and digital assets for the Business Technology Solutions (BTS) Change Management and Training Team.
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Samaritan Healthcare is live with EPIC and we are seeking a Clinical Informatics Specialist to serve as a resource in promoting the understanding, integration, and application of information technology for our Samaritan Healthcare community in sunny, Moses Lake, Washington.
Full-timeRemoteExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is seeking a Senior Director, Regulatory Affairs to join a leading health information technology and clinical research organization.
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Senior Director, Regulatory Affairs - Permanent - Remote. In this role, you will provide leadership and advice on the development of optimum regulatory strategies for drug development, product lifecycle management and portfolio management, particularly focused on emerging biopharmaceutical company customer goals in oncology.
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Integrate strategic regulatory & drug development support services into emerging biopharmaceutical company clinical trial offerings. Support engagements with regulatory authorities (e.g., FDA, EMA) on behalf of customers, across the lifecycle of drug development from pre-clinical to licensing, including contribution to briefing documents and other meeting materials, and attendance and contribution to meetings and other interactions.
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Strategic regulatory experience in novel oncology investigational product development to registration including interactions with US and European regulatory authorities. Lead assessments of risk and probability of regulatory success and development of mitigations for candidate pharmaceutical products, including providing regulatory contributions to indication prioritization exercises, development strategy evaluations and gap analyses, due diligence, and similar activities.
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Typically requires 15-20+ years relevant clinical research and/or regulatory experience with multi-regional and global focus including significant experience in senior strategic role, including specific oncology investigational product experience.
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Strategic leadership of the development of regulatory submissions, including INDs, marketing/licensing authorizations (NDA/BLA/MAAs), special designations (orphan drugs, pediatrics plans, "fast-track. Interface with clients in collaboration with existing Therapeutic Science & Strategy Unit Centres of Excellence to provide strategic advice and incorporate regulatory guidance.
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