• Work as Principal Clinical Data Standards Specialist at Novartis
    Principal Clinical Data Standards Specialist is responsible for the development, maintenance and implementation of Industry CDISC and regulatory compliant Clinical Data Standards, providing expert support to business users and teams on their use in line with the Clinical Data Standards strategy.
  • Apply Online for Senior Product Specialist at Novartis - B.Pharm, BSc Apply
    Develop business plans and implement related activities like customer events, sales & marketing campaigns, sales presentations necessary to achieve agreed objectives.
  • Novartis Require Regulatory Coordinator - Chemistry, Pharmacy, Biochemistry, Biotechnology Degree Apply
    Contributes and support the development of submission of product registration, progress reports, supplements, amendments, and/or periodic experience reports.
  • Novartis Hiring Senior QA Expert
    Supplier qualification: Ensures a valid Quality Agreement in line with the requirements of the Novartis global template is in place and continuously amended to the business needs.
  • Novartis Require SFMC Quality Specialist
    BTech / Masters in Technology or Masters in Business Administration. The Execution QA comprehensively reviews rendering quality, Metadata, Content Matrices. Novartis
  • Novartis looking for Principal Scientific Writer | M.Pharm, MSc Apply
    Working in partnership with the Client Engagement team, Medical Communications, and the Writing delivery team for a designated client group/therapeutic area (TA) / brand, this role will be responsible for delivering and supporting scientific excellence of Medical Communications services across their accounts
  • Work as RA CMC Associate Manager at Novartis
    Responsible for regulatory activities specifically related to chemistry, manufacturing, and control (CMC). Activities such as the preparation and publication of REG CMC documentation for submissions to Health Authorities.
  • Work as Clinical Trial Associate at Novartis
    Designs and coordinates the overall direction of clinical development projects. Coordinates activities of associates and investigators to ensure compliance with protocol and overall pre-clinical objectives. Maintains a high level of professional expertise through familiarity with clinical literature and participates in project team meetings
  • Require Quality Specialist at Novartis
    Execution QA comprehensively reviews rendering quality, Metadata, Content Matrices accuracy with the email build, Subscriber segmentation, Journey configurations, and deployment accuracies. Calls out and communicates all inconsistencies to Campaign Managers and Deployment teams.
  • Novartis looking for Product Specialist
    Sales experience in Healthcare / Pharma / related business, established Network to target Customer Group desirable. Territory knowledge is must.
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