• Sr . Clinical Trial

    University of Pennsylvania (Philadelphia, PA)
    …technology/systems required to enhance clinical research operations. In this role, the Sr Clinical Trial Project Manager will independently manage ... of health and wellness programs and resources, and much more. Posted Job Title Sr . Clinical Trial Project Manager (Center for Cellular Immunotherapy) Job… more
    University of Pennsylvania (10/27/24)
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  • Clinical Study Team Lead

    Pfizer (Collegeville, PA)
    …Therapeutic Areas. Your project management skills will be leveraged to develop clinical trial timelines and oversee budgets for the assigned clinical ... Medicine, Anti-Infectives, or Inflammation & Immunology preferred. + Broad experience in a Clinical Trial Execution discipline (eg senior study management… more
    Pfizer (11/14/24)
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  • Clinical Trial Supply Senior

    CSL Behring (King Of Prussia, PA)
    **The Opportunity** The Clinical Trial Supply (CTS) Senior Study Manager manages the end-to-end supply chain for assigned clinical studies throughout the ... multi-year study lifecycle. The CTS Senior Study Manager independently leads clinical studies...to clinical sites and patients. + Develop clinical trial supply documents and training to… more
    CSL Behring (10/30/24)
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  • Sr . Quality Specialist

    Insight Global (Malvern, PA)
    …-Outstanding EM issues -Transfer of document to the EM -Status of Clinical Trial Material (CTM) lots/production schedule -Various workstreams (help build ... our large pharmaceutical clients is looking to hire a Sr Quality Specialist to join the EQ team. The...team, and help to ensure that all quality-related activities project goals and deadlines are met. In particular, the… more
    Insight Global (11/09/24)
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  • Sr . CRA/CRA 2, Glioblastoma and Pediatric…

    IQVIA (Wayne, PA)
    …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines *… more
    IQVIA (10/15/24)
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  • Sr . Director - CMC Development

    Lilly (Philadelphia, PA)
    …Operations) in the planning and execution of a manufacturing strategy to meet clinical trial supply requirements. + Manage the creation of, and lifecycle, ... organizations (CMO) globally to ensure reliable and sufficient supply to Avid/Lilly clinical trials. + Develop, implement, and execute upon supply chain strategy for… more
    Lilly (10/31/24)
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  • Senior Specialist, Clinical Supply…

    Merck (West Point, PA)
    …as the GCS spokesperson at clinical development related meetings (ie, Clinical Trial Teams) and product development related meetings. The incumbent must ... but are not limited to:** + Participates as a key stakeholder on the Clinical Trial Teams (CTT) and collaborates closely with other functional area… more
    Merck (11/08/24)
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  • Senior Specialist, Clinical Supplies…

    Merck (West Point, PA)
    …activities include, but are not limited to:** + Participates on the Clinical Trial Team(CTT)and collaborates closely with other functional area representatives ... Trade, Distribution, Operations etc.) as well asother organizations such as Global Clinical Trial Operations (GCTO) Regional colleagues and Global Development… more
    Merck (11/08/24)
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  • Senior Scientist, Biomarker Operations,…

    Merck (Upper Gwynedd, PA)
    …include, but are not limited to: + Collaborate closely with biomarker scientists and project teams to plan clinical trial biomarker set-up using logistical ... **Preferred Experience and Skills:** + Drug discovery experience, including familiarity with clinical trial execution in Oncology studies + Biomarker assay… more
    Merck (11/05/24)
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  • Senior Associate, Senior Database…

    Pfizer (Collegeville, PA)
    …of drug development process and data operations required for the reporting of clinical trial data (eg data review, study reports, regulatory submissions, safety ... in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities… more
    Pfizer (11/07/24)
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  • Manager, Senior Clinical Data…

    Pfizer (Collegeville, PA)
    …of consistent, efficient, and quality processes to meet timelines and deliverables. + Serve as Clinical Data Scientist and Trial Lead for one or more clinical ... discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and... Practices (GCDMP), and related regulatory requirements + Strong Project and Risk Management + Strong verbal and written… more
    Pfizer (10/23/24)
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  • Late-Stage Clinical Development Leader

    Organon & Co. (Plymouth Meeting, PA)
    …Officer, and is accountable for: + The leadership of the following teams: Global Clinical Development (GCD), Clinical Trial Operations (CTO), Clinical ... issues and risks. + As member of the Organon Senior Leaders team contributing by driving our Company into...other areas. + Leadership of the following teams: Global Clinical Development, Clinical Trial Operations,… more
    Organon & Co. (09/10/24)
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  • Clinical Data Manager II

    System One (King Of Prussia, PA)
    Title: Sr CDM II Location: King of Prussia, PA Onsite...- Direct with the client If you are a Senior Clinical Data Manager with experience working at ... the lead study data manager for a large, complex trial or multiple, smaller studies. Will support CDM process...Team, work collaboratively with cross-functional team members to meet project deliverables with quality and per agreed timelines *… more
    System One (10/31/24)
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  • Senior Principal Scientist, Biostatistics…

    Merck (Upper Gwynedd, PA)
    …+ Lead research activities for innovative statistical methods and applications in clinical trial development. + Collaborates in publication of research results ... oral and written reports to effectively communicate results of clinical trials to the project team, our...R. + Solid understanding of worldwide regulatory requirements and clinical trial expertise from phase II to… more
    Merck (11/08/24)
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  • Senior Statistical Programmer, Late Stage…

    Merck (North Wales, PA)
    …or related field and at least 5 years SAS programming experience in a clinical trial environment or + MS in Computer Science, Statistics, Applied Mathematics, ... position is a key collaborator with statistics and other project stakeholders in ensuring that project plans...at least 3 years SAS programming experience in a clinical trial environment. **Required Skills:** + Effective… more
    Merck (11/09/24)
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  • Director, Clinical Statistics

    Teva Pharmaceuticals (West Chester, PA)
    …highly knowledgeable with respect to statistical principles, engaged with innovative clinical trial methodology, and experienced with appropriate software and ... clinical development and Global Statistics through the use of novel/innovative clinical trial designs and statistical methodology + Becomes proficient in the… more
    Teva Pharmaceuticals (08/22/24)
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  • AVP/Section Head, Metabolism - Global…

    Merck (North Wales, PA)
    …optimal trial design and monitoring of studies, producing high-quality clinical documents and presentations. The position requires a solid understanding of the ... excellence in the late development of assets within the Metabolism Section of Global Clinical Development + May serve as a senior therapeutic area content expert… more
    Merck (10/25/24)
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  • Clinical Research Coordinator C (Department…

    University of Pennsylvania (Philadelphia, PA)
    …will develop study protocols, manage contracts and IRB regulatory issues, and oversee clinical trial data management. CRC-C will assist team of research ... Clinical Research Coordinator-C who will take on a senior research role within the Traumatic Brain Injury ...brain injury. CRC-C will take an active role in project oversight, supported by clinical research assistants… more
    University of Pennsylvania (10/27/24)
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  • Senior Scientist, Statistical Programming

    Merck (North Wales, PA)
    …years of experience with all of the following: SAS programming in a clinical trial environment including data steps, procedures, SAS/MACRO, and SAS/GRAPH; ... potential medical breakthroughs. + Review the quality and reliability of clinical studies using deep scientific knowledge, statistical analysis and high-quality data… more
    Merck (08/21/24)
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  • Senior Issue Lead, Inspection Management…

    Pfizer (Collegeville, PA)
    …inspection experience + Process and system management experience + Detailed knowledge of clinical trial processes and relationships required + Knowledge of GCP ... The " Senior Issue Lead, Inspections" will be accountable to...inspection responsibilities around: + Directing asset/study team colleagues within CS&O/ Clinical to ensure successful inspection and audit outcomes +… more
    Pfizer (11/08/24)
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