• Manager , Global Trade Compliance

    Takeda Pharmaceuticals (Cambridge, MA)
    …of export and import compliance policies and procedures for the organization regarding Clinical Trial Material (CTM) and raw material shipments. + Manage daily ... Ensure adherence to country specific standard operating procedures for importing/exporting clinical trial material and raw materials, including logistics,… more
    Takeda Pharmaceuticals (09/17/25)
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  • Lead Clinical Research Coordinator

    Fresenius Medical Center (Mishawaka, IN)
    …Mishawaka, IN as this position is on-site.** PURPOSE AND SCOPE: Assists with clinical trial activity, site profit and loss, subject enrollment strategy, and ... and team meetings . Trains to review or negotiate clinical trial contracts, confidentiality disclosure agreements and... clinical research staff accurate utilization of the Clinical Trials Management System . Participates and… more
    Fresenius Medical Center (09/11/25)
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  • Clinical Research Coordinator Data Focused

    University of Colorado (Aurora, CO)
    …Level or CRC I:** + Assist with and oversee the day-to-day operations of clinical trials and studies + Independently abstracts and records all research subject ... protocol onto protocol-specific Case Report Forms (CRFs) and into clinical trials database in an accurate and...criteria, and confirms eligibility of subject to participate in clinical trial + Perform informed consent process… more
    University of Colorado (09/14/25)
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  • Medical Support Assistant (Advanced) Specialty…

    Veterans Affairs, Veterans Health Administration (Marion, IL)
    …care provider and/or specialty care provider (MD, NP, PA),registered nurse care manager , clinical associate (LPN or medical assistant/health technician) and an ... identifying and developing ways to resolve problems with the administrative and clinical staff on access, customer service, patient flow, revenue, and data… more
    Veterans Affairs, Veterans Health Administration (09/25/25)
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  • Category Manager - IT

    US Tech Solutions (Tarrytown, NY)
    …such as but not limited to Laboratory, Radiology, Perioperative, Medical-Surgical and clinical capital purchasing. The Category Manager will develop sourcing ... offer optimal balance of cost quality and outcomes. + The category manager will be responsible for developing market analysis, benchmarking comparisons and… more
    US Tech Solutions (07/18/25)
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  • Clinical Scientist, Hematology

    Bristol Myers Squibb (Madison, NJ)
    …assigned project to execute activities associated with the conduct + May serve as Clinical Trial Lead for one or more trials + May lead or support trial ... Will be responsible for design and execution of assigned clinical trial activities and work closely with...perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of… more
    Bristol Myers Squibb (09/19/25)
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  • Senior Manager , Data, Analytics and AI…

    Bristol Myers Squibb (Princeton, NJ)
    … Data Ecosystem (CDE) that primarily delivers technology strategy and solutions for clinical trial execution, data management and data review capabilities (eg ... and unique perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency,… more
    Bristol Myers Squibb (09/15/25)
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  • Medical Director, Clinical Development,…

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …and database research on clinical trials as needed + Collaborates with Clinical Project Managers and Clinical Trial Managers at the study level and ... Oncology is a qualified physician scientist with exceptional academic clinical trials ' experience, preferably in solid tumor...of clinical study concepts which lead to clinical trial protocols and is responsible for… more
    Regeneron Pharmaceuticals (09/22/25)
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  • Clinical Research Contracts Associate

    Dana-Farber Cancer Institute (Brookline, MA)
    …collaboration with Manager and Director , confidentiality agreement, clinical trial agreements, consortium agreements, multi-site and academic subcontract ... inquiries from PIs , study teams , OHRS and other parties on non-complex clinical trial related matters, requiring Director input and support. + Drafts written… more
    Dana-Farber Cancer Institute (09/20/25)
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  • Senior Principal Scientist, Clinical

    Abbott (Sylmar, CA)
    …will be viewed as a leader on scientific and medical matters related to clinical trial design, clinical evaluations, risk management, strategy, management, ... writing/managing clinical evaluation (plans and reports) or clinical trial protocols, risk master lists, ...organization, and some interactions with principal investigators in the trials . + Responsible for the delivery of the development… more
    Abbott (08/08/25)
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