• Regional Clinical Research Associate (Remote)

    Teleflex (Minneapolis, MN)
    …disciplines. * Minimum five years as a CRA in the medical device or pharmaceutical industry or with a CRO. **Specialized Skills / Other Requirements** * ... Demonstrated aptitude and knowledge in relevant therapeutic area. Vascular Interventional Cardiology is strongly preferred. * Experience conducting monitoring activities for first in human, investigational device exemption, post-approval and/or post-market… more
    Teleflex (09/12/25)
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  • Program Manager, Immunology

    IQVIA (New Providence, NJ)
    …and Abilities:** Proficient in PC applications. Business acumen (knowledge of the pharmaceutical industry , including the applications for IQVIA data) Change ... management/process analysis skills. Strong communication skills, including ability to train, present and deal tactfully with clients. Project management experience in overseeing or contributing in difficult, multi-discipline projects Managerial skills,… more
    IQVIA (09/12/25)
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  • Manager, Technical Lead, Project Management CSO…

    Bristol Myers Squibb (New Brunswick, NJ)
    …life sciences, or related field + 5 years relevant experience in the pharmaceutical industry or related healthcare environment. + Knowledge of ERP/MRP (SAP) ... systems and supply chain principles highly preferred. + Experience in cGMP environment, preferably clinical. + Demonstrates ability to plan, manage and execute multiple projects and to deliver against critical timelines in a fast-paced, rapidly changing… more
    Bristol Myers Squibb (09/12/25)
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  • Program Director (Remote)

    WCG Clinical (Cary, NC)
    …managing multiple programs & efforts simultaneously + 5+ years of experience working on pharmaceutical industry projects requiring 21 CFR Part 11 Compliance + 3+ ... years of experience in Account Management/Client Relationship Management + Background in Clinical Research and technology preferred + Excellent interpersonal & organizational skills and able to effectively communicate with cross-functional teams and at all… more
    WCG Clinical (09/12/25)
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  • Quality Engineer

    Abbott (Santa Clara, CA)
    …years (+) experience in Quality Assurance/Quality Engineering from medical device or pharmaceutical industry . + Sufficient knowledge in test method validations & ... statistical analyses. + Regulations experience in any: 21 CFR 820, FDA, 13485, 14971. + Proven experience in relevant areas of Quality, Regulatory or Engineering, preferably within a medical device environment + Advanced knowledge of relevant regulations is… more
    Abbott (09/12/25)
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  • Package Developer

    Coty (Sanford, NC)
    …degree with equivalent experience in design and testing within consumer goods and/or pharmaceutical industry + ASQ Certified Quality Inspector (CQI) or ISTA ... Laboratory Professional CPLP Technician Certification or equivalent is preferred + 5+ years' experience in a laboratory environment, preferably with package testing laboratory + 3+ years' experience in a manufacturing environment **Working Knowledge:** + 49… more
    Coty (09/12/25)
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  • Global Head of Hematology (Medical Affairs)

    Sanofi Group (Cambridge, MA)
    …Clinical experience is highly valuable + Minimum of 10 years of experience in the pharmaceutical industry , with at least 5-7 years in medical affairs + Proven ... track record in global medical affairs leadership, preferably in hematology or oncology + Strong understanding of the global healthcare landscape, particularly in hematologic malignancies + Excellent leadership skills with the ability to inspire and develop… more
    Sanofi Group (09/11/25)
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  • Senior Director, Quantitative Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …Lead in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led ... company. To do this, we empower our people to realize their potential through lifechanging work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive,… more
    Takeda Pharmaceuticals (09/11/25)
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  • Documentation Specialist

    Catalent Pharma Solutions (St. Petersburg, FL)
    …in the systems and maintaining the systems) required 1+ years in the pharmaceutical industry is preferred. + 1+ years' experience authoring electronic batch ... record recipes is preferred. + 1+ years of experience authoring written and electronic batch record recipes is preferred. + Individual may be required to sit for long periods of time, while reading or preparing documents. The individual may also be required to… more
    Catalent Pharma Solutions (09/11/25)
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  • Director I, Aesthetics Clinical Development

    AbbVie (Irvine, CA)
    …deliverables + At least 5 years of clinical trial experience in the pharmaceutical industry , academia, or equivalent. + Knowledge of clinical trial methodology, ... regulatory and compliance requirements in Aesthetic Medicine. + Ability to interact externally and internally to support global scientific and business strategy. Must possess excellent oral and written English communication skills. Additional Information… more
    AbbVie (09/10/25)
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