Medical Information Specialist
Novartis
Job Description Summary Sandoz is going through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines.Now as an independently listed company, Sandoz aims to increase its strategic focus, operate with greater agility, set clearer business objectives, enhance shareholder returns, and strengthen its culture for us, the Sandoz associates. This is an exciting time in our history, and by creating a new and ambitious path, it will provide a unique opportunity for us all, both professionally and personally.Job DescriptionIn line with overall product strategy, the medical information specialist is responsible for execution of medical information tasks as first line enquiry handling, and advanced case management in accordance with Sandoz procedures. This position is reporting to the Head Medical Operations at Sandoz Nordics.Your Key Responsibilities:Your responsibilities include, but are not limited to:Perform Medical Information Service according to Sandoz procedures and standards, and in collaboration with and the medical information team for Sandoz Nordics and other relevant functions.Ensure medical enquiries are responded to in a high quality, timely manner, and in accordance with, and fulfilling applicable standardsEnsure medical insights are provided to cross functional groups, including, but not restricted to: Pharmacovigilance, Regulatory affairs, Market Access, QA, Commercial teams, Brand team and others.Responsible for risk identification and assessment, mitigation planning as well as implementation and monitoring of appropriate internal controls within the area of responsibilities.Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receiptWhat you’ll bring to the role:Essential Requirements:Profound knowledge of Medical information managementCollaborating across boundaries.Operations Management and Execution.Project Management.Transferring scientific and clinical data into appropriate medical information responsesSkills:General knowledge of:Sandoz medicinal product portfolioGxP working environmentOrganization Skills.Patient Care.Stakeholder Engagement.Functional people managementLanguages :Danish (or Swedish)EnglishYou’ll receive:Competitive salary and Bonus based on personal and company results; Pension Scheme; Health Insurance; Flexible working conditions with hybrid working policy; Employee recognition scheme; Development both professionally and personally; Learning about company processesWhy Sandoz?Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, touched the lives of almost 500 million patients last year and while we are proud of this achievement, we have an ambition to do more!With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.Our momentum and entrepreneurial spirit is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is encouraged!The future is ours to shape!Commitment to Diversity & Inclusion:We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.Join our Sandoz Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Sandoz and our career opportunities, join the Network here:#SandozSkills Desired Clinical Research, Clinical Trial Protocol, Clinical Trials, Database Administration, Lifesciences
København
Fri, 28 Feb 2025 23:35:15 GMT
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