• Global Clinical Data

    Merck (Sacramento, CA)
    …our existing and pipeline products to produce safe, effective, innovative medicine. The Global Clinical Data Standards Vocabulary Specialist, Associate ... Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical...Vocabulary Specialist may lead or participate in:** + Internal clinical data standards forums +… more
    Merck (04/20/24)
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  • Senior Director, Global Clinical

    Merck (Sacramento, CA)
    …ensuring successful delivery of projects on time, within budget, and meeting quality standards . You will play a critical role in driving the strategic direction of ... + Bachelor's Degree with at least fifteen (15) years of pharmaceutical, clinical drug development, project management and/or medical field experience. Or + Master's… more
    Merck (05/01/24)
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  • Associate Director, Clinical Quality…

    Merck (Sacramento, CA)
    …+ Develops, updates, and maintains GCP inspection procedures and guidelines within Global Clinical Trial Operations (GCTO). + Contributes to the development ... . It is business critical that our Company receives consistent, accurate, high-quality data from clinical trials conducted worldwide. In collaboration with the … more
    Merck (04/24/24)
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  • Ultrasound Clinical Account Specialist…

    J&J Family of Companies (Sacramento, CA)
    Ultrasound Clinical Account Specialist - San Jose, California - Biosense Webster, Inc. - 2406168592W **Description** Biosense Webster, Inc., a member of Johnson & ... Johnson's Family of Companies, is recruiting for an Ultrasound Clinical Account Specialist to support the San Jose, Sacramento,...electrophysiology. For more than 30 years, we've been the global market leader in the science and technology of… more
    J&J Family of Companies (04/30/24)
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  • Senior Clinical Research Associate - NH,…

    Merck (Sacramento, CA)
    …country clinical research law & guidelines. + Excellent understanding of Global , Country/Regional Clinical Research Guidelines and ability to work within ... ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as… more
    Merck (05/01/24)
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  • Senior Electronic Data Capture Engineer

    Takeda Pharmaceuticals (Sacramento, CA)
    …Create and own database build SOPs and processes. The EDC Engineer will work with Data Management and Standards teams to implement new processes as well as ... with leaders to resolve issues affecting the delivery of clinical trials + Collaborate with standards team...development process. + Minimum of 10+ years' experience in Data Management, Programming, Clinical IT, or other… more
    Takeda Pharmaceuticals (03/23/24)
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  • Global Head of IT Digital & Commercial…

    Envista Holdings Corporation (Sacramento, CA)
    …'Go To Market' Omnichannel approach (incl enabling B2B, B2C, DTC etc.); Consumer Data Acquisition & Offer Management; PIM / DAM & Brand; Website Consolidation & ... Management. We are looking for a Global Head of IT Digital & Commercial Platforms to...commercial platforms and ensure compliance with the policies and standards + Monitor and evaluate digital performance and outcomes,… more
    Envista Holdings Corporation (02/21/24)
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  • Manager, Feasibility

    Takeda Pharmaceuticals (Sacramento, CA)
    …international equivalent required; in a life science preferred, + 4+ years in Clinical Operations, Data Analytics, global feasibility, and trial optimization ... + Develop strong analytical competencies including the use of clinical data sets to facilitate trial planning,...of direct responsibility in leading strategic feasibility assessments of global clinical research studies at a sponsor… more
    Takeda Pharmaceuticals (02/24/24)
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  • Senior Manager, Feasibility

    Takeda Pharmaceuticals (Sacramento, CA)
    … research setting at a sponsor or CRO. + 6+ years of experience in Clinical Operations, Data Analytics, global feasibility, and trial optimization with ... data -driven feasibility assessments for Phase I - IV clinical studies, including protocol design optimization, country/site feasibility and selection, enrollment… more
    Takeda Pharmaceuticals (02/24/24)
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  • Associate Director, GMP Quality Control

    Sumitomo Pharma (Sacramento, CA)
    …and suppliers of drug substances and drug products used for investigational clinical trials and/or commercial phases. The Associate Director ensures compliance with ... GMPs, SMPA procedures and applicable global Regulatory guidelines by providing oversight and management of...expiry date is available to support commercial product and clinical program needs. **Job Duties and Responsibilities** + Represent… more
    Sumitomo Pharma (04/19/24)
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  • Sr CRA/Principal CRA - Cell or Gene Therapy…

    ThermoFisher Scientific (Sacramento, CA)
    …that people and communities depend on - now and in the future. Our global Clinical Operations colleagues within our PPD(R) clinical research services ... meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission...letters in a timely manner using approved business writing standards . Escalates observed deficiencies and issues to clinical more
    ThermoFisher Scientific (05/02/24)
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  • Medical Science Liaison - Vaccines (Southern…

    Sanofi Group (Sacramento, CA)
    …further data collection by: + MSLs support development and execution of clinical trials. + MSLs identify potential data sources and develop partnerships for ... experts and decision-makers engaging in mutual scientific exchanges to accelerate data dissemination. Sanofi's Medical Field base teams enhance the understanding of… more
    Sanofi Group (05/01/24)
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  • Executive Director, Commercial Supply Chain

    Sumitomo Pharma (Sacramento, CA)
    …will be responsible for the oversight, management, and integration of the global commercial supply chain organization. This role will provide leadership and vision ... Supply Chain: + Ensuring the ongoing supply of commercial products in all global markets + End-to-end value chain planning - Inventory management across raw… more
    Sumitomo Pharma (04/04/24)
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  • Director, Business Development - Regulatory…

    Cardinal Health (Sacramento, CA)
    …experts who provide consulting services in a myriad of capacities, including: + Global Regulatory Strategy Development + Global Regulatory Affairs + Chemistry ... Manufacturing and Controls Development + Nonclinical Development and Consulting + Clinical Development and Research + Medical Writing + Regulatory Publishing +… more
    Cardinal Health (03/27/24)
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