• Ultimate (Irvine, CA)
    …an Associate Documentation Specialist, who will assist the Medical Affairs /Clinical Science team in the development of clinical documents for clinical ... source documents, ensuring reviewer comments are addressed) on Medical Affairs /Clinical Science deliverablesComplete brief writing projects (eg tables, summaries,… more
    CareerBuilder (02/20/21)
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  • PRA Health Sciences (Irvine, CA)
    …with yearly merit and performance reviews. Responsibilities The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative ... with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements. This role will focus on Car-T Oncology / Hematology… more
    Jobs2Careers (03/03/21)
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  • Kavo Kerr Regulatory Affairs

    Envista Holdings Corporation (Orange, CA)
    …**Operating Company:** Kerr **Job Description:** **JOB SUMMARY:** The **Kavo Kerr** ** Regulatory Affairs Associate ** is responsible for supporting ... monthly status reports on status of current issues to the Manager of Regulatory Affairs . + Assists with Customs requests. + Assists in the assembly of global… more
    Envista Holdings Corporation (02/13/21)
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  • International Associate Regulatory

    Medtronic (Northridge, CA)
    International Associate Regulatory Affairs Specialist (APAC) Location: Northridge, California, United States Requisition #: 21000679 Post Date: 1 day ago ... **INTERNATIONAL ASSOCIATE REGULATORY AFFAIRS SPECIALIST (APAC)** The Diabetes Operating Unitfocuses on improving the lives of those within the global… more
    Medtronic (03/06/21)
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  • Regulatory Affairs Specialist

    Kelly Services (Santa Ana, CA)
    Kelly Science & Clinical is currently hiring an entry level ** Regulatory Affairs Specialist** to support a long-term engagement at one of our Global Med Device ... more effective and efficient. **Responsibilities:** Prepares, dispatches and files routine Regulatory Affairs documentation, including but not limited to 30-day… more
    Kelly Services (02/24/21)
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  • Assistant/ Associate Scientific Director

    AbbVie (Irvine, CA)
    …YouTube (https://www.youtube.com/user/AbbVie) and LinkedIn (https://www.linkedin.com/company/abbvie) . ** Associate /Assistant Scientific Director, Medical Affairs ... ** **Job Description** The Associate /Assistant Director, Medical Affairs has a key role within the BOTOX Therapeutic...regulatory , etc.) as they relate to on-going medical affairs projects. * Represents AbbVie at external meetings including… more
    AbbVie (03/06/21)
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  • Associate Manager, Program Management

    Edwards Lifesciences (Irvine, CA)
    …Strong leadership skills and ability to influence stakeholders. + Background in regulatory affairs and project management within the biopharmaceutical or medical ... As a new product development ** Associate Manager, Program Management** , you will lead...market segments preferred + At least 1 year in Regulatory Affairs and Clinical studies. + Knowledge… more
    Edwards Lifesciences (02/18/21)
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  • Associate Director, Strategic…

    Abbvie (Irvine, CA)
    Affairs activities** by providing marketing input to R&D, Medical Affairs , Regulatory , Clinical, Business Development and Manufacturing functions. ... the right questions and driving results. All while wearing jeans to work! ** Associate Director, Strategic Communications** **YOU ARE more than just a title, YOU ARE… more
    Abbvie (01/20/21)
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  • Associate Director, Global Publications…

    AbbVie (Irvine, CA)
    …and LinkedIn (https://www.linkedin.com/company/abbvie) . JOB SUMMARY: The Associate Director, Global Publications will oversee development of ... guide the team's decisions regarding scientific communications. Interfaces with Medical Affairs and Clinical leadership of assigned TAs to ensure successful… more
    AbbVie (01/28/21)
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  • Associate Director, Clinical Pharmacology

    Pfizer (San Diego County, CA)
    …We emphasize on the candidate's quantitative pharmacology skills, scientific reasoning, regulatory affairs skills, written and verbal communication skills, ... special group dosing etc) to the clinical and Development teams and in regulatory documentation. + Leads clinical pharmacology contributions to all regulatory more
    Pfizer (02/27/21)
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  • Clinical Research Associate

    Endologix, Inc (Irvine, CA)
    …clinical objectives. + Under the direction of the Sr. Manager, Clinical Affairs , implement clinical research projects. + Oversee patient screening and enrollment at ... Clinical Trial data in EDC + Track all the Regulatory documents in CTMS (Clinical Trial Management System) +...duties as assigned by supervisor + Knowledge of FDA regulatory requirements related to the conduct of clinical studies.… more
    Endologix, Inc (01/24/21)
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  • Associate Manager, Medical Writing…

    Edwards Lifesciences (Irvine, CA)
    …timelines, and resolving project-related issues with cross-functional partners (eg, Regulatory Affairs , Quality, Clinical Project Managers, Clinical Data ... Management, Biostatistics, etc.) * Act as a technical expert to key stakeholders to develop and lead the implementation of corporate, business unit, and departmental process updates and improvements (eg, MDR compliance, etc.) * Provide direction and guidance… more
    Edwards Lifesciences (03/04/21)
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  • Associate Director Search & Evaluation…

    AbbVie (Irvine, CA)
    …of multiple aspects of drug development (eg, pre-clinical research, clinical development, Regulatory Affairs , Chemistry Manufacturing and Controls (CMC)). + Must ... posses basic understanding of the aesthetics portfolios and advances in the science of aging. + Must possess basic knowledge of generally accepted Business Development practices, eg financial, contracting, governance review. + Strong Project management/… more
    AbbVie (01/28/21)
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  • Forecasted Opportunity: Senior Specialist,…

    Edwards Lifesciences (Irvine, CA)
    …minimum job requirements, you will receive additional information about our Clinical Affairs Talent Community. The Senior Clinical Research Monitor will ensure trial ... patients' safety by assuring trials are conducted ethically and within regulatory compliance, data accuracy, and protocol adherence. **Key Responsibilities:** +… more
    Edwards Lifesciences (01/30/21)
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  • Intern, Legal

    MicroVention, Inc. (Aliso Viejo, CA)
    …the direction of the Associate General Counsel and Senior Director of Legal Affairs to gain hands-on professional experience in the practice of law. You might be ... HR, HR Communications, Talent Development, Marketing, R&D, Manufacturing, Quality, Regulatory , Accounting, and more. **Legal Intern** The **Legal Intern** will… more
    MicroVention, Inc. (02/22/21)
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  • Medical Director, Eye Care

    AbbVie (Irvine, CA)
    …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and emerging issues. ... of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses and other program documents. + Responsible,… more
    AbbVie (01/31/21)
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  • Director, Evidence Solutions

    AbbVie (Irvine, CA)
    …therapeutic or functional areas. This includes projects originating from Medical Affairs , HEOR, or Epidemiology assigned directly to the Director and those ... assigned to departmental Trial Managers. Under the supervision of the Associate VP of GMTM, the Director ensures alignment of new projects with product strategic… more
    AbbVie (03/06/21)
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  • Executive Director, Marketing

    AbbVie (Irvine, CA)
    …within the body contouring franchise. The Executive Director, reports to the Associate Vice President of Marketing, and is responsible for the development, analysis ... strategies for capital equipment and consumable businesses. + Collaborate with Regulatory , Medical, Legal, Compliance in development of all promotional pieces and… more
    AbbVie (03/04/21)
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