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    Job · 19511319

    Eli Lilly and Company logo

    Scientific Writer/Senior Scientific Writer- Quality Review

    Eli Lilly and Company · Bengaluru · onsite · Posted 24d ago

    Undisclosed4–12 yrsfulltimeSourced fromNaukri

    About a minute. You'll make an account on the way through.

    About this role

    Job Summary

    At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

    Purpose: The purpose of the Scientific Writer/Senior Scientific Writer role (Quality review and document finalization) is to support the Global Scientific Communications team and other functions to produce documents of high quality.

    Responsibilities

    • Scientific Communications Document Support
    • Ensure timely delivery of error-free, high-quality documents that meet international standards of written English
    • Correct errors in grammar, style, formatting, and syntax. Identify and fix flaws in logic and flow
    • Follow style guides/templates provided by the team
    • Follow best-practice based on Lilly internal standards
    • Verify data against source files, ensure accuracy and consistency of data and content within and between related documents
    • Document finalization/publishing services
    • Produce final eCTD-compliant PDFs of medical regulatory documents using publishing software
    • Review and format Word files to ensure as many compliance requirements are in the source file as possible
    • Render the Word files into PDFs
    • Review the PDFs and edit them as needed to ensure that all regulatory requirements are met

    General expectations

    • Maintain a strong customer focus
    • Accountable for achieving timelines by managing activities efficiently and proactively; utilize ability to understand and apply team communication strategies to work products
    • Coach new staff or others requiring development in core areas
    • Coordinate with vendors if any of the aforementioned activities are outsourced

    Process efficiency and technology advancement

    • Maintain proficiency in applicable software, tools, processes, and workflows
    • Use creativity to introduce new tools, processes, and structure to accomplish broader organizational goals and meet standards while providing solutions to streamline team workflow
    • Improve document processes by establishing uniform cross-organizational practices; suggest process or tool enhancements to improve effectiveness and minimize redundancy between databases and other tools

    Therapeutic Disease State Management

    • Understand key priorities and communication strategies across therapeutic areas and/or organizational units
    • Maintain a working knowledge of product and disease state information
    • Continue to develop therapeutic knowledge and be familiar with trial design, rationale and data. Apply this knowledge in activities listed above

    Minimum Qualification Requirements

    • Bachelors degree
    • Strong written and verbal communication skills in English
    • Demonstrated ability to communicate and negotiate solutions to complex technical challenges with cross-functional colleagues, external vendors and customers
    • Demonstrated project management and time management skills
    • Cognitive abilities, including verbal reasoning, attention to detail, critical thinking, and analytical ability
    • Interpersonal skills and the ability to be flexible in varying environments
    • Ability to utilize high-level end-user computer skills (e.g., word processing, tables and graphics, spreadsheets, presentations and templates)
    • Ability to work well independently and as part of a team, within and across culturally and geographically diverse environments
    • Proven ability to assemble, share and apply key learnings across multiple projects

    Other Information/Additional Preferences

    • Knowledge of medical and statistical terminology; willingness to expend effort in acquiring scientific knowledge and understand strategic issues
    • General knowledge of scientific literature search and retrieval
    • Limited travel, up to approximately 10%


    Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

    Sourced from naukri

    Skills

    interpersonal skillsQuality Documentationprocess efficiencyQuality ReviewworkflowProject ManagementGraphicstime managementanalyticalpublishing

    About Eli Lilly and Company

    Eli Lilly and Company logo

    Eli Lilly and Company

    Pharma

    2.7k+

    employees

    1993

    33 years old

    Indianapolis, Indiana

    United States (USA)

    ₹23.4L PA avg

    Avg at Eli Lilly and Company

    About

    Lilly unites caring with discovery to create medicines that make life better for people around the world.

    Industries

    Pharma

    Employee ratings

    10 reviews

    3.7/ 5

    Culture

    2.2

    Career growth

    2.0

    Work-life

    3.3

    Employees rate it well for

    Work-Life Balance39Job Security38

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    Scientific Writer/Senior Scientific Writer- Quality Review · waiting for your command