• AI Solutions Manager, Life Sciences R&D…

    Deloitte (Pittsburgh, PA)
    …and data mapping + Experience with solutions for data-driven trials and clinical development insights (ie: site burden, patient burden, study feasibility, ... solutions + 4+ years of experience with Life Sciences Pharmaceutical R&D clinical data lifecycle. Experience to include introducing new technologies like GenAI,… more
    Deloitte (10/24/25)
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  • Investigator Contracts Lead - FSP

    Parexel (Harrisburg, PA)
    …with Investigative Site contracting and compensation requirements + Interacts with clinical site contracts & legal contacts, client and partner legal team, ... + Work with partners to develop and oversee the global site budget process + Work with clinical trial sites and directly negotiate cost, business and contractual… more
    Parexel (11/19/25)
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  • Physical Therapy Faculty | Tenure Track Fall 2026…

    slippery rock university (Slippery Rock, PA)
    …within the program curriculum. These responsibilities include: leading the program's clinical education team, facilitating clinical site affiliation ... agreements, developing and sustaining relationships with clinical site staff, counseling and mentoring students regarding clinical education needs and wants,… more
    slippery rock university (11/24/25)
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  • Senior Statistical Programmer- Analysis…

    Merck (North Wales, PA)
    …staff + Active in professional societies VETJOBS \#EBRG BARDS2020 SPjobs **Required Skills:** Clinical Site Management, Clinical Testing, Data Analysis, Data ... programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data, transform the data into… more
    Merck (11/07/25)
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  • Senior Scientist, Statistical Programming

    Merck (North Wales, PA)
    …partners, and keeping current with industry submission data standards including SDTM, ADaM, clinical site data for CDER inspection planning, etc. + Responsible ... deliverables for world-wide regulatory application submissions of drug and vaccine clinical development projects. + Be accountable for submission data standards… more
    Merck (10/23/25)
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  • Clinical Consultant - Post Go-Live…

    Oracle (Harrisburg, PA)
    …and system performance Healthcare & Informatics Expertise * Deep understanding of clinical workflows, informatics principles, and site readiness requirements * ... **Job Description** Overview: The Site Project Manager is responsible for local ...(preferred) * 5+ years of experience in healthcare IT, clinical informatics, or EHR implementation/project management (required) * Experience… more
    Oracle (11/25/25)
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  • Lead Clinical Consultant

    Oracle (Harrisburg, PA)
    …perfectly with both project objectives and specific site requirements. + ** Site Readiness Leadership** : Offer your clinical expertise and leadership to ... **Job Description** **Oracle Health Government Services** **Lead Clinical Consultant** **Location: United States** **No visa sponsorship...content, and tailoring it to meet specific project and site needs. You will be at the heart of… more
    Oracle (11/25/25)
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  • Medical Group Education Coordinator…

    Penn State Health (Camp Hill, PA)
    …and information to begin the clerkship. + Facilitate student rotations, assignments, and clinical site placements in collaboration with faculty and clinical ... operation of the PSCOM clerkship program, APP and GME clinical rotations. It serves as a critical liaison with...point of contact for the OME and PA Program clinical year team, ensuring compliance with institutional policies, academic… more
    Penn State Health (11/15/25)
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  • Oncology Late Stage Clinical Scientist…

    Pfizer (Collegeville, PA)
    …study level informed consent documents, and contributes to authoring of IBs, site training materials, clinical study reports, regulatory responses, and other ... responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for...requiring you to live within commuting distance and work on- site an average of 2.5 days per week. The… more
    Pfizer (11/16/25)
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  • Clinical Drug Supply Manager

    ICON Clinical Research (Blue Bell, PA)
    …reviews IVRS user manuals; Designs, reviews and approves IP-related study tools (for clinical study teams and investigative site use), as needed. Supports ... Clinical Drug Supply Manager ICON plc is a...travel passes, health assessments, among others. Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON… more
    ICON Clinical Research (11/05/25)
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