Associate, Global Scientific Communications (GSC), Document Delivery at Eli Lilly and Company

Indianapolis, Indiana, United States

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceuticals, HealthcareIndustries

Requirements

Correct errors in grammar, style, formatting, and syntax; identify and fix flaws in logic and flow
Follow style guides/templates provided by the team and Lilly internal standards
Verify data against source files, ensure accuracy and consistency of data and content within and between related documents
Collaborate with global counterparts and track document metrics across groups
Produce final eCTD-compliant PDFs using publishing software; review and format Word files for compliance; render to PDFs and edit as needed
Provide editorial and project management support, including formatting, proofreading, rendering, bookmarking
Conduct literature searches; obtain and process copyright transfer and authorship agreements
Verify data and references for accuracy; create figures and diagrams
Write cover letters to journal editors; coordinate translation and/or validation
Handle systems of record (e.g., DataVision, RIM, Planisware Book of Work) with data steward/project management responsibilities
Support encoring efforts across therapy areas, functions, and regions by editing, adapting word counts, and completing publication procedures
Coordinate workload and work assignments with DDH Air Traffic Control direction locally and globally

Responsibilities

Ensure timely delivery of error-free, high-quality documents that meet international standards of written English
Provide leadership, internal coordination, and guidance as a member of the GSC Document Delivery Hub (DDH)
Partner across Global Scientific Communications (GSC) and key partners to ensure documents meet all guidelines, Lilly policies, and external requirements
Participate in producing electronically compliant documents for regulatory submissions (e.g., FDA/EMA) and publication deliverables (manuscripts, posters/presentations)
Work with writing teams to establish and supervise key milestone timelines
Edit documents for style/usage and content
Ensure all steps of the submission process are driven
Achieve time-bound deliverables (as described in the truncated description)

Skills

Scientific Communications

Document Delivery

Grammar Correction

Style Editing

Formatting

Syntax Correction

Regulatory Submissions

FDA Compliance

EMA Compliance

Manuscript Preparation

Poster Design

Presentation Development

Eli Lilly and Company

Develops and delivers prescription medicines globally

About Eli Lilly and Company

Eli Lilly and Company is a global pharmaceutical company that focuses on discovering, developing, and delivering medicines to improve health. The company has a long history of scientific achievements, including the creation of insulin, the first life-saving treatment for diabetes. Lilly's operations involve extensive research and development to create new medications and enhance existing ones, ensuring they are safe and effective. Their products are primarily prescription medicines sold to healthcare providers for various medical conditions, including diabetes, cancer, and pain management. What sets Lilly apart from its competitors is its strong commitment to ethical practices and the protection of its products from counterfeiting. The company's goal is to enhance lives through innovative medical solutions while maintaining high standards of quality and ethics.

Indianapolis, IndianaHeadquarters

1876Year Founded

$1,180.1MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Competition from Novo Nordisk's Ozempic may impact tirzepatide's market share.

Potential construction delays in Indiana could affect GLP-1 drug production timelines.

Regulatory challenges may hinder Kisunla's expansion in new Alzheimer's markets.

Differentiation

Eli Lilly's rich history includes the first life-saving insulin treatment.

Lilly's strategic partnerships enhance its position in neurodegenerative disease treatments.

FDA approval of Zepbound opens new therapeutic markets for sleep disorder treatments.

Upsides

Lilly's $9 billion complex in Indiana boosts GLP-1 drug production capacity.

Kisunla's approval in China expands Lilly's Alzheimer's treatment market in Asia.

Collaboration with EVA Pharma enhances Lilly's reputation as socially responsible.

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