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    Expert Scientific Writer

    Novartis
    8+ years years
    Preffered by Company
    Hyderabad
    Not Disclosed July 9, 2024
    Job Description
    Job Type: Full Time Education: Master’s degree in Life Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology or Biophysics) or a degree in Dentistry or Bachelor degree in Veterinary Sciences (B.V.Sc.) Skills: Causality Assessment, Communication Skills, GCP guidelines, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    Expert Scientific Writer

     

    Job ID: REQ-10007897
    Posted On: May 22, 2024
    Location: Hyderabad, India (Hybrid)
    Division: Operations
    Business Unit: CTS
    Company/Legal Entity: IN10 (FCRS = IN010) Novartis Healthcare Private Limited
    Functional Area: Research & Development
    Job Type: Full-time
    Employment Type: Regular
    Shift Work: No

     

    Summary

    The Expert Scientific Writer manages and completes assigned Medical Communications projects at high quality standards and within agreed timelines. Projects include manuscripts, abstracts, posters, slide sets, satellite symposia content, congress or advisory board reports, publication planning, and medical education materials for internal medical and/or clinical teams.

     

    Key Responsibilities

    • Project Management: Manage and complete assigned Medical Communications projects, ensuring high quality and adherence to timelines.
    • Content Creation: Prepare literature reviews, abstracts, posters, slide sets, and complex manuscripts using various data sources, including clinical study reports, patient profiles, and protocols.
    • Quality Control: Perform quality control (QC) checks and proofreading to meet customer expectations.
    • Multi-Project Handling: Manage multiple projects for up to two brands simultaneously, implementing customer management tactics based on feedback.
    • Compliance: Adhere to and support the group's project management tools, standards, policies, and initiatives. Follow Novartis specifications for documentation (Novstyle, templates, etc.) and track clinical trial milestones for assigned projects.
    • Record Maintenance: Maintain records for all assigned projects, including archiving, and ensure audit, SOP, and training compliance.
    • Training: Train new joiners and fellow colleagues as required.
    • Additional Tasks: Perform additional tasks as assigned.

     

    Commitment to Diversity & Inclusion

    Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

     

    Role Requirements

    Essential Requirements

    • Minimum science degree or equivalent (B.Sc./equivalent) with 10 years of Clinical Research (CR) experience, or M.Sc./M.Pharma with 8 years of Clinical Research (CR) experience.
    • Excellent written and oral English skills.

     

    Desirable Requirements

    • Extensive experience in Clinical Research.
    • Proficiency in scientific writing and medical communications.

     

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