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    Associate Medical Writer

    Novo Nordisk
    2+ years
    Not Disclosed
    Bangalore
    10 Nov. 22, 2024
    Job Description
    Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    About Novo Nordisk

    Novo Nordisk is a global healthcare leader with over 100 years of expertise in combating serious chronic diseases. Our legacy, particularly in diabetes care, drives us to expand and reach millions of patients globally, impacting over 40 million lives every day. With 63,000 employees worldwide, we aim to be life-changing by fostering collaboration, innovation, and dedication. Join us to contribute to a transformative mission that goes beyond healthcare to change lives.

    Department Overview: Global Medical Affairs – Global Business Services (GMA-GBS)

    GMA-BLR is an extension of Global Medical Affairs from Novo Nordisk’s headquarters in Denmark, and is a part of the Global Business Services (GBS) unit in Bangalore, India. The Regions and Operations vertical within GMA-BLR collaborates with global regions and affiliates to support and execute real-world studies through their life cycle, from protocol development to study conduct, data analysis, publications, and medical affairs activities.

    Position: Associate Medical Writer

    Location: Bangalore, India
    Department: Global Medical Affairs – Global Business Services (GMA-GBS)

    As an Associate Medical Writer at Novo Nordisk, you will play a crucial role in supporting the medical writing efforts for clinical studies and medical communications. Your responsibilities will include drafting and reviewing study protocols, study reports, and other key clinical documents. Additionally, you will engage in the development of scientific content for conferences, publications, and internal/external activities.

    Key Responsibilities

    • Medical Writing Tasks:

      • Prepare key documents such as study protocols, non-interventional study reports, and investigator brochures in collaboration with global medical directors.
      • Write abstracts, congress posters, and presentations for scientific and medical events.
      • Create publication proposals in line with standard Novo Nordisk templates.

    • Document Coordination:

      • Moderate discussions with study groups for the development of study protocols and study reports.
      • Coordinate clinical document version reviews and the approval process to ensure compliance with timelines and regulations.

    • Literature Searches:

      • Conduct literature searches and prepare summaries for systematic literature reviews.

    • Cross-Functional Collaboration:

      • Engage in internal and external marketing and medical activities, such as expert meetings, lectures, and conferences.
      • Contribute to the ongoing improvement of cross-functional and global collaboration, sharing best practices and knowledge across teams.

    • Audit-Preparedness:

      • Ensure audit readiness and contribute to maintaining audit-preparedness for medical documentation.

    Qualifications

    We are looking for candidates who meet the following qualifications:

    • Education:

      • Degree in a relevant field (e.g., life sciences, medical, pharmaceutical).

    • Experience:

      • 2+ years of experience in medical writing, with particular expertise in study protocols, non-interventional study reports, and investigator brochures.
      • Experience with real-world studies and therapy areas such as diabetes, obesity, and MASH.
      • Strong skills in performing literature searches and preparing summaries of findings.

    • Skills:

      • Proficiency in developing abstracts, posters, and presentations for scientific conferences.
      • Excellent communication and collaboration skills to work across global teams.
      • Experience in ensuring audit-preparedness and managing clinical document reviews.
      • Familiarity with regulatory requirements and guidelines in the medical writing process.
      • Knowledge of process improvements and knowledge sharing in a global setting.

    Working at Novo Nordisk

    Novo Nordisk is committed to creating a life-changing impact on the lives of patients worldwide. By joining us, you will become part of a dynamic and innovative environment where we are shaping the future of healthcare together. We embrace collaboration, creativity, and diversity to ensure that our work makes a real difference in the lives of people around the globe.

    Application Process

    To apply, please submit your CV and motivational letter through our online application tool.

    Deadline: 30th November 2024

    Important Disclaimer

    Beware of fraudulent job offers that may pose as Novo Nordisk recruiters. Novo Nordisk does not extend unsolicited job offers or request personal information, payments, or fees during recruitment processes. Always verify offers through our official channels.

    Commitment to Diversity and Inclusion

    At Novo Nordisk, we are committed to fostering an inclusive culture that values diversity in all forms. We believe that the diverse backgrounds, experiences, and perspectives of our employees contribute to our success and innovation. We are committed to providing equal opportunities for all job applicants. Together, we are life-changing.

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