Eli Lilly and Company is hiring for the Associate – Medical Writing position in Bengaluru, Karnataka. The role focuses on developing regulatory documents that support clinical development and product registration, including clinical study reports, clinical trial protocols, regulatory responses, and marketing authorization applications.
Candidates with a bachelor’s degree in a scientific or health-related field and experience in technical, regulatory, or scientific writing can apply. Experience in clinical development, clinical trials, regulatory affairs, and medical writing is preferred.
Job Details
| Particulars | Details |
|---|---|
| Company | Eli Lilly and Company |
| Job Title | Associate – Medical Writing |
| Job Requisition ID | R-111668 |
| Job Location | Bengaluru, India |
| Job Type | Full-time |
| Qualification | Bachelor’s degree in a scientific, health, communications, or technology-related field |
| Experience Requirement | Demonstrated experience in technical, regulatory, or scientific writing |
| Application Deadline | October 30, 2026 |
| Application Mode | Online |
Position: Associate – Medical Writing
The selected candidate will work with cross-functional and multidisciplinary teams to develop accurate, scientifically supported regulatory documents for clinical development and product registration.
Key document types include:
- Clinical trial protocols
- Clinical study reports
- Regulatory briefing documents
- Regulatory responses
- Investigational New Drug (IND) applications
- Marketing authorization applications
Responsibilities
- Collect, evaluate, and organize scientific data and inputs from multiple sources to develop document content.
- Draft, edit, review, and finalize regulatory and clinical development documents.
- Ensure scientific accuracy, consistency, clarity, and completeness across related documents.
- Coordinate scientific reviews, consolidate reviewer comments, and incorporate feedback.
- Manage document development timelines and communicate project progress to stakeholders.
- Identify potential delivery risks and coordinate with cross-functional teams to ensure timely completion.
- Maintain knowledge of therapeutic areas, drug development, regulatory guidelines, and publication standards.
- Support scientific presentations, process improvements, knowledge sharing, and document management activities.
Eligibility and Qualifications
Candidates must meet the following minimum requirements:
- Bachelor’s degree in a scientific, health, communications, or technology-related field.
- Demonstrated experience in technical, regulatory, or scientific writing.
- Strong written and verbal communication skills.
- Successful completion of a writing exercise during the candidate evaluation process.
Preferred Qualifications
- Graduate degree with a formal research component or a degree in life sciences.
- Experience writing regulatory documents, clinical trial documents, or scientific publications.
- Knowledge of clinical development, clinical trial processes, or regulatory activities.
- Therapeutic-area expertise in neuroscience, oncology, cardiovascular, immunology, endocrinology, or other relevant fields.
- Strong project management and time management skills.
- Proficiency in word processing, tables, graphics, spreadsheets, presentations, and templates.
Required Skills
- Medical and scientific writing
- Regulatory document development
- Clinical research documentation
- Scientific data interpretation
- Editing, proofreading, and quality checks
- Cross-functional stakeholder coordination
- Project and timeline management
- Regulatory and publication guideline knowledge
- Written and verbal English communication
- Document management and presentation preparation
