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Lilly Sr. Assoc Manager-Medical Writing-BEST in Bengaluru, India

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

1. Content Strategy and Execution: Document Preparation, Development and Finalization/Document Management

  • Effectively collect and evaluate data, information, and input from multiple sources, functions, and regions to create a cohesive content strategy for writing projects.

  • Plan (including organizing/preparing outlines), write (including first-draft authoring), edit, review, coordinate, and complete the regulatory documents supporting clinical development/product registration.

  • Conduct effective document initiation meeting to ensure authoring team alignment and understanding.

  • Build scientific-based rationale that support the purpose of more complex and/or strategic documents.

  • Ensure data are presented in a clear, complete, accurate, and concise manner.

  • Ensure that key data, statements and conclusions are consistent across related documents, and that statements and conclusions are integrated, accurate, balanced and supported by appropriate data.

  • Coordinate expert/scientific reviews, collate reviewer’s comments, adjust content of document as required based on internal/external input, and prepare final version.

  • Ensure and coordinate quality checks for accuracy.

  • Exhibit flexibility in moving across development and preparation of multiple document types.

  • Influence or negotiate change of timelines and content with other team members.

  • Work with internal and external experts to develop and prepare presentations.

  • As needed, may build and manage relationships with vendors/alliance partners.

2. Project and Stakeholder management

  • Lead the writing process and apply effective project management skills to ensure timely completion of high-quality regulatory documents.

  • Build/communicate credible writing project timelines.

  • Anticipate and mitigate risks to delivery.

  • Work with teams and stakeholders to ensure smooth and timely development of documents and escalate issues, as appropriate, to ensure document completion.

  • Effectively communicate project status to stakeholders.


  • Bachelor’s degree in a scientific, health, communications, technology health related field.

  • Demonstrated experience in technical/ regulatory scientific writing.

  • Strong communication and interpersonal skills.

  • Successful completion of writing exercise (a writing exercise is required as part of the candidate evaluation process)

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At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people.​ We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe!