• Paralegal

    State of Massachusetts (Woburn, MA)
    …to trials. Specific duties include: * Assist in case preparation, pretrial and trial preparation, both in and outside the courtroom * Compile and analyze case ... and databases * Locate victims and witnesses * Assemble trial exhibits * Create maps, diagrams, and layouts for...diagrams, and layouts for use as visual aids for trial * Review legal forms for accuracy * Coordinate… more
    State of Massachusetts (12/18/25)
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  • Programming Project Leader

    Sanofi Group (Cambridge, MA)
    …clinical development (ie understanding of statistical concepts, techniques and clinical trial principles) and ability to manage and lead regulatory submissions. + ... + Master degree and 4+ years of programming experience preferably in processing clinical trial data in the pharmaceutical industry. + Bachelor degree and 6+ years of… more
    Sanofi Group (12/18/25)
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  • Paralegal

    Robert Half Legal (North Reading, MA)
    …contract role, you will play a pivotal part in supporting attorneys with trial preparation, legal research, and case management. This position is ideal for an ... civil litigation and family law. Responsibilities: * Assist attorneys with trial preparation, including gathering and organizing relevant documentation. * Conduct… more
    Robert Half Legal (12/11/25)
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  • Data Strategy Lead, CVRM

    Genentech (Boston, MA)
    …shaping and implementing innovative, multi-modal data strategies that enhance trial design, support regulatory and commercial needs, and accelerate decision-making. ... lead multi-modal data strategies across CVRM that integrate real-world data, clinical trial data, digital endpoints, and operational metrics + You ensure data… more
    Genentech (12/10/25)
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  • Vice President, Real World Evidence

    Chiesi (Boston, MA)
    …R&D: + Partner closely with R&D to integrate RWE into Phase 3 trial design, ensuring robust evidence generation for regulatory submissions through external control ... validation. + Identify opportunities to use RWD to optimize trial protocols, patient recruitment, and endpoint selection. + Support...+ Deep understanding of Phase 3, 3b, and 4 trial design, regulatory requirements, and market access strategies. +… more
    Chiesi (12/09/25)
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  • Jury Commissioner

    State of Massachusetts (Adams, MA)
    …sets forth policies, guidelines and forms for the selection and management of grand and trial jurors in furtherance of the objectives of GL c. 234A; * Oversees the ... *SALARY* The salary range for this position is $138,323.12 ( Trial Court EXM, Step 1) to $196,002.82 ( Trial...( Trial Court EXM, Step 1) to $196,002.82 ( Trial Court EXM, Step 8). Starting salary is commensurate… more
    State of Massachusetts (12/04/25)
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  • Associate Director, Biostatistics

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …study/project team member, provide statistical input in different perspective of the clinical trial conduct such as CRF review, IRT setting, DMC set up, annual ... + Reviews clinical, statistical, and regulatory literature for current clinical trial results, regulatory trends and new statistical methods to be applied… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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  • Product Liability Litigation Adjuster

    CVS Health (Boston, MA)
    …with and overseeing outside counsel. + Participating in meetings and attending mediation and trial as necessary to oversee and assist in the defense or resolution of ... litigated claims for an insurance carrier or corporation, including mediation experience and trial exposure. + 3-5 years of legal or claims experience. + Familiarity… more
    CVS Health (11/22/25)
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  • Principal Product Manager, Growth

    PagerDuty (Boston, MA)
    …In this pivotal role, you'll own the end-to-end user journey from trial acquisition through paid conversion and platform adoption for existing customers across ... growth products and services. + Lead vision, strategy, and execution for trial -to-paid conversion as well as existing customer optimization across Operations Cloud… more
    PagerDuty (11/20/25)
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  • Associate Director, Clinical & Quality Process…

    Takeda Pharmaceuticals (Boston, MA)
    …considered. + Enable a compliant quality system in safety and clinical trial delivery systems via CPMQ continual improvements projects. Actively participate and ... represent in continual improvement projects, related to safety and clinical trial delivery in partnership with GDO, PSPV, GRA etc. Review the outputs of the safety… more
    Takeda Pharmaceuticals (11/14/25)
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