• Program Lead II, Clinical Program Development

    AbbVie (Irvine, CA)
    …strategic advocate for pipeline assets and provides operational reality to our scientific experiments via scientific expertise, strategic thinking, a global ... who support clinical trial execution and the Development and Global Medical Affairs Therapeutic Area MDs/SDs. + Key contributor to the portfolio planning process… more
    AbbVie (07/11/25)
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  • Senior Biotatistician

    Abbott (Alameda, CA)
    …- Demonstrates extensive understanding of statistical concepts and methodologies SCIENTIFIC REPORTS AND PUBLICATIONS - Responsible for Statistical Methods section ... accurate and timely answers to routine questions from clients, and scientific insight when answering nonstandard questions - Responsible for maintaining good… more
    Abbott (07/03/25)
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  • Sr. Product Marketing Manager, Kcentra

    CSL Behring (King Of Prussia, PA)
    …and manage the core promotional strategy, peer-based promotional plan and HCP scientific education plan. This role requires the marketer to manage and execute ... education activities + Leading cross-functional support team members including medical affairs , insights & analytics, corporate accounts and the field sales… more
    CSL Behring (07/03/25)
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  • Senior Manager, Statistics

    AbbVie (South San Francisco, CA)
    …areas of work may include clinical trials, patient safety, and global medical affairs . The Senior Manager works independently in partnership with experts in multiple ... leadership for design, analysis and reporting for clinical or other scientific research programs.Independently develop protocols and statistical analysis plans (or… more
    AbbVie (06/24/25)
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  • Regulatory Program Management Specialist…

    Genentech (South San Francisco, CA)
    …the moments that matter. **The Opportunity** We're looking for a Regulatory Affairs Professional to join our Product Development Regulatory (PDR) team, specialising ... Are** + You hold a Bachelor's degree and bring experience in regulatory affairs , preferably with a focus on labelling + You're well-versed in Good Pharmacovigilance… more
    Genentech (09/20/25)
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  • Clinical Trial Operations Development Program

    AbbVie (North Chicago, IL)
    …Operations group conducts/manages clinical trials and provides therapeutically aligned, scientific strategy and operations management for the planning, execution and ... clinical development, quality assurance, technology, data management, and regulatory affairs . + Study Management Associate Organization: The Study Management… more
    AbbVie (09/20/25)
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  • Director, R&D Program Management

    Organon & Co. (Jersey City, NJ)
    …**Required Education, Experience and Skills** + Bachelor's degree in a scientific , life science, technical discipline, or relevant field. Advanced degree preferred. ... experience​ in R&D functions (eg, Clinical Research, Early Development, Medical Affairs , Pharmacovigilance, Regulatory Affairs , etc.), experience in women's… more
    Organon & Co. (09/20/25)
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  • Full Professor

    North Carolina Central University (Durham, NC)
    …acquire and learn to apply their problem-solving skills, technology-based training, and scientific concepts, to appreciate and improve the quality of life. The ... departmental faculty colleagues systematically, provide for the conduct of departmental affairs in an orderly manner through department meetings and the appointment… more
    North Carolina Central University (09/19/25)
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  • Associate Director, Social Media Strategy

    Gilead Sciences, Inc. (Foster City, CA)
    …team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve ... **Stakeholder Engagement & Enablement** + Coordinate with internal teams (Public Affairs , Marketing, HR, Business Units) to source content and amplify enterprise… more
    Gilead Sciences, Inc. (09/19/25)
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  • Submission Manager, Global Submission Management…

    Sanofi Group (Cambridge, MA)
    …is required. **Qualifications:** + Bachelor's degree, or equivalent, in regulatory affairs , the sciences, or related areas of study, and relevant experience ... 5 years of experience in the pharmaceutical industry, with direct regulatory affairs experience. + High degree of knowledge regarding the dossier assembly/production… more
    Sanofi Group (09/19/25)
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