Medical Affairs – Medical Writing
Eli Lilly and Company
Full time- 2+ years
- Not Disclosed
- Bengaluru, India
- Post Date: Mar 27, 2024
- End Date: May 27, 2024
- 2+ years
- Not Disclosed
- Bengaluru, India
- Post Date:Mar 27, 2024
- End Date: May 27, 2024
Skills:
- pharma
- Medical Writing
- Clinical Trial
Job Description:
Responsibilities
- 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.
Qualification & Experience
- Graduate degree with formal research component or in life sciences.
- Demonstrated mastery of verbal and written English skills in the medical, scientific or technical writing fields.
- Clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience specific to hiring area (e.g., neuroscience, oncology, cardiovascular, immunology or endocrine expertise).
- Experience writing regulatory, clinical trial documents and/or publications
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Salary
Not Disclosed
-
Role
Medical Writer
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Area of Practice
- Medical Writing
- Medical Affairs
-
Experience
2+ years
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