• Director, Third Party Data Acquisition

    Takeda Pharmaceuticals (Boston, MA)
    …like MaxisIT CT Renaissance + Understanding multiple data formats used in technologies like Veeva EDC , Rave or Inform EDC , eCOA, IRT, eConsent, Telehealth. + ... responsible for timely and high-quality delivery of systems and documentation for non- EDC data in support of Clinical studies. + Conduct oversight of implementation,… more
    Takeda Pharmaceuticals (09/21/25)
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  • Clinical Research System Specialist

    Dana-Farber Cancer Institute (Brookline, MA)
    …successfully interface to downstream clinical systems, including COE, BOE, BICs, EMPI and InForm EDC . OnCore CTMS Quality Control + Review data in the ... OnCore CTMS for accuracy, completeness, and compliance with DF/HCC policies. + Monitor OnCore QC reports and facilitate timely resolution of error flags. + Track expiration of protocols and automatic closures in OnCore and update posted documents on OncPro, as… more
    Dana-Farber Cancer Institute (09/20/25)
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  • Director, Office of Data Quality-Clinical Research

    Dana-Farber Cancer Institute (Brookline, MA)
    …CTRP and Clinicaltrials.gov + Quality control and governance of CRF data in DF/HCC Inform EDC + Quality control of subject registrations and operational data in ... the OnCore CTMS + Feasibility review and activation of submissions in the iRIS PRMS + Maintenance of DF/HCC policies and procedures + DF/HCC educational initiatives, training sessions, educational resources, and e-learning library + Monitor, track, and report… more
    Dana-Farber Cancer Institute (08/23/25)
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  • Sr. Clinical Research Coordinator

    Actalent (Bronx, NY)
    …which can come from clinical research, school, or nursing. + Experience with multiple EDC systems, with Medidata and Inform highly preferred. + Robust experience ... in data management, as 60% of the job involves data management and coordination. + Experience recruiting, screening, and consenting patients for clinical trials. Work Environment The position requires working on-site in the Bronx four days per week. Please… more
    Actalent (09/11/25)
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  • Clinical Study Build Programmer

    Lilly (Indianapolis, IN)
    …Part 11 etc. + Knowledge of industry standard clinical technologies including CTMS, EDC (Veeva CDMS preferred, Rave, InForm ), eCOA, IxRS, Clinical Data ... Repositories, etc. + Knowledge of CDISC and CDASH standards/standard terminology + The ability to work independently as well as in a team environment. + Project and Vendor management experience + Excellent time management skills and a proven ability to work on… more
    Lilly (07/30/25)
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  • Clinical Research Analyst

    Kelly Services (Kansas City, MO)
    …+ Ensure proper data entry within operational platforms, ie, Electronic Data Capture EDC System and Customer Relationship Management CRM System. + Data Analysis: + ... and developments in the field of clinical research to inform and improve study design and data analysis. +...data entry within operational platforms ie Electronic Data Capture EDC System and Customer Relationship Management CRM System Data… more
    Kelly Services (09/22/25)
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  • Clinical Trial Manager

    Bristol Myers Squibb (Princeton, NJ)
    …the Clinical Trial Management System (CTMS) is current and complete, and access to eDC and vendor systems is available for the country and clinical trial site ... competing priorities + Interpersonal, oral and written communication skills to influence, inform or guide others + Good verbal and written communication skills (both… more
    Bristol Myers Squibb (09/24/25)
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  • Principal Clinical Data Science Lead

    ICON Clinical Research (Blue Bell, PA)
    …must have experience with at least one of ICON's preferred CDMS (eg Rave, Inform , Oracle Clinical, OCRDC, UX EDC ) + Highly computer literate, including strong ... documents and will be responsible for the maintenance, cleaning, and lock of the EDC study databases + Review the project contract in order to ensure that any… more
    ICON Clinical Research (09/13/25)
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  • Senior Director, Head of Feasibility, Americas

    BeOne Medicines (San Mateo, CA)
    …of care, disease prevalence, drug landscape, and historical trial data, to inform protocol development and establish geographic footprints and proposed sites for ... Trial Diversity teams **Computer Skills:** Microsoft Office Suite, CTMS applications, EDC applications, analytic tools (eg Citeline, Trialtrove, etc.) and additional… more
    BeOne Medicines (09/11/25)
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  • Associate Director - Safety Data Scientist

    Lilly (Indianapolis, IN)
    …+ Manages and analyzes complex datasets across multiple platforms (eg LSS, Mosaic, Inform , Veeva, FAERS) in order to assess business issues and drive analytic ... existing regulations/guidelines and trends for GPS automation and technology (ie e2B, eDC , AI, safety mailings) to proactively drive change to maintain compliance. +… more
    Lilly (09/23/25)
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