• Principal Biostatistician FSP, Early Phase

    IQVIA (Durham, NC)
    …you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor systems. These sponsor ... experts. + Write statistical analysis plans. + Monitor internal and CRO project activities including timelines, deliverables, and availability of resources. +… more
    IQVIA (08/19/25)
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  • Principal Pharmacometrician, FSP

    IQVIA (Durham, NC)
    …This affords all the benefits of working for an industry leading global CRO while operating within a sponsor team and utilizing sponsor systems. These sponsor ... Collaborate on projects and innovations with industry leaders in the Pharma and CRO sectors. + Cohesive team environment fostering a collaborative approach to study… more
    IQVIA (08/14/25)
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  • Principal Research Associate (Biomarker…

    Teva Pharmaceuticals (West Chester, PA)
    …a minimum of 3 years of experience in the biotech/biopharma or CRO industry. . Experience in biomarker assay method development, qualification/validation and sample ... Qualifications . At least 5 years of experience in biotech/biopharma or CRO . In-depth knowledge of ligand binding assays and other bioanalytical methodologies… more
    Teva Pharmaceuticals (08/09/25)
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  • Principal Biostatistician FSP, Neuroscience

    IQVIA (Durham, NC)
    …get all the benefits of working for an industry leading global CRO while collaborating directly with expert cross-functional sponsor teams. Sponsor clients include ... experts. + Write statistical analysis plans. + Monitor internal and CRO project activities including timelines, deliverables, and availability of resources. +… more
    IQVIA (07/10/25)
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  • Associate Clinical Project Manager

    Sumitomo Pharma (Boise, ID)
    …meetings - ie Study Team Meetings, Investigator Meetings, Monitors' workshops and CRO Training + Prepares and delivers program/study updates as determined by project ... the delivery of clinical trial supplies in collaboration with CRO and other team members + Supports CPM with...SOPs + Maintains knowledge of oncology therapeutic area, current medical practice and pharmaceutical regulations in order to ensure… more
    Sumitomo Pharma (09/23/25)
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  • Veterinary Technician I - $5,000 Sign On Bonus!

    Charles River Laboratories (Reno, NV)
    …treatment records and perform, track and schedule follow-ups. + Maintain appropriate medical records for each animal in accordance with study and regulatory ... collegiate veterinary technology program accredited by the American Veterinary Medical Association Committee on Veterinary Technician Education and Training… more
    Charles River Laboratories (09/22/25)
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  • Digital Product Portfolio Head

    ThermoFisher Scientific (Guilford, CT)
    …business of Thermo Fisher Scientific is a leading provider of global CRO solutions. We provide comprehensive drug development, laboratory and lifecycle services to ... customers across pharmaceutical, biotechnology, medical device, academic and government entities. By harnessing innovative technology and expertise, we work to… more
    ThermoFisher Scientific (09/20/25)
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  • Senior Director, R&D Business Ops Lead

    CSL Behring (King Of Prussia, PA)
    …and resource capacity planning for business alignment.​ **The Role** + Manage CRO partnerships across clinical trials​​ + Communicate with Sourcing, Legal to support ... in R&D contracts, procurement, or R&D vendor management​​ + Knowledge of CRO /vendor management​​ + Experience with SOW development and legal terms​​ + Experience… more
    CSL Behring (09/16/25)
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  • Principal Biostatistician FSP, Late Phase

    IQVIA (Durham, NC)
    …yields all the benefits of working for an industry leading global CRO and collaborating directly with cross-functional sponsor teams. Sponsor clients include world ... experts. + Author statistical analysis plans. + Monitor internal and CRO project activities including timelines, deliverables, and availability of resources. +… more
    IQVIA (09/11/25)
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  • Director, Regional Clinical Study Management…

    BeOne Medicines (San Mateo, CA)
    …process for assigned region in collaboration with feasibility managers, country heads, medical affairs and any other stakeholders. + Provides regional input on ... Report in collaboration with Global Clinical Study Manager and Medical Writing. **Quality** _Study management responsibilities:_ + Anticipates potential concerns… more
    BeOne Medicines (09/11/25)
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