• cGMP Testing/QC Manager

    Element Materials Technology (Ann Arbor, MI)
    …technical objectives. The ideal candidate will possess strong expertise in Quality Control operations and quality systems, with a focus on compliance, process ... continuous improvement. This is an exciting opportunity for an experienced Quality Control and cGMP Sample Analysis Leader to contribute significantly to a growing… more
    Element Materials Technology (03/26/25)
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  • Associate Director, Feasibility

    Takeda Pharmaceuticals (Boston, MA)
    …feasibility, and trial optimization with evidence of increasing responsibility within a pharmaceutical company, CRO or relevant industry vendor required. + 7 ... reporting to the Director, Feasibility. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led… more
    Takeda Pharmaceuticals (05/26/25)
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  • Executive Director - Therapeutic Area Operations…

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    …teams and ensuring execution against the risk management plan. + Oversee CRO partnership related to delivery of outsourced services, including ensuring that CTM ... staff provide an appropriate and documented level of oversight for site/ CRO /vendor services + Actively participate in appropriate governance meetings and acts as… more
    Regeneron Pharmaceuticals (05/22/25)
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  • Study Associate I, Clinical Operations

    Taiho Oncology (Princeton, NJ)
    …of relevant clinical trial support or site management experience in the pharmaceutical , biotechnology, CRO and/or healthcare industry. + Experience and knowledge ... KPIs and performs quality review of the eTMF (per CRO oversight plan) while collaborating with internal and CRO study teams to resolve any issues and risks. +… more
    Taiho Oncology (04/05/25)
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  • Associate Director, CRA Functional Manager

    BeOne Medicines (Emeryville, CA)
    …ICH and associated regulatory guidelines + > 5 years of management or oversight within pharmaceutical or CRO Industry + 4-5 > 5 years of (CRA) monitoring ... experience in the pharmaceutical or CRO Industry + Excellent communication and interpersonal skills + Excellent organizational skills and ability to prioritize… more
    BeOne Medicines (05/27/25)
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  • Senior Research Scientist (Epidemiologist, Safety…

    ThermoFisher Scientific (Frederick, MD)
    …**Environmental Conditions** Office **Job Description** Evidera is a business within Pharmaceutical Product Development, LLC (PPD) a leading global contract research ... organization ( CRO ). We provide integrated scientific expertise and global operational...of products. The Evidera Data Analytics team supports the pharmaceutical / biotechnology/ medical device companies throughout the product lifecycle,… more
    ThermoFisher Scientific (05/23/25)
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  • Analytical Chemistry Scientific Director…

    Lilly (Indianapolis, IN)
    …and engineers while offering access to world-class capabilities for pharmaceutical development. **Position Responsibilities:** Scientists in this position will be ... leading analytical efforts within an innovator organization focused on pharmaceutical product development and commercialization with specific focus on small… more
    Lilly (04/28/25)
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  • Manager / Senior Manager, CMC Project Management

    WuXi AppTec (Natick, MA)
    …PhD in Chemistry or Pharmaceutical Sciences + 2+ years of pharmaceutical or CRO /CMO industry experience preferred + Project management experience preferred ... **Overview** STA Pharmaceutical , a WuXi AppTec Company, has an exciting...deliverables. Define project tasks and resource requirements. + Closely monitor/ control project progression to ensure projects are completed on… more
    WuXi AppTec (05/13/25)
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  • Associate Director, Clinical Research, Value…

    Takeda Pharmaceuticals (Lexington, MA)
    …partner with TA Project Managers as necessary. + Oversees & manages external CRO partners accountable to support operational execution of IIR work. **MACS and ... for line management of Senior Managers, as well as contractors or CRO service providers. + Orchestrates the involvement of appropriate cross-regional or… more
    Takeda Pharmaceuticals (05/03/25)
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  • Biostatistics Manager, Biosimilar Development

    Amgen (Washington, DC)
    …+ Provides statistical contributions, statistical review and quality control of Study Concept Documents (SCDs), protocols, randomization specifications, ... and other communications in close partnership with CROs in a full-service CRO model. + Influences study design and defends statistical approaches internally and… more
    Amgen (05/19/25)
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