Medical Writing Job at Eli Lilly
Are you passionate about regulatory writing and eager to make a difference in the pharmaceutical industry? The Associate, GSC Regulatory role at Eli Lilly offers an exciting opportunity to engage with multidisciplinary teams and lead the development of critical documents for regulatory audiences. This Medical Writing Job in Bengaluru involves crafting high-quality regulatory documents such as protocols, clinical study reports, and marketing authorisation applications. With a focus on effective project management and collaboration, this role is essential in ensuring timely completion and clarity in document presentation. Join Eli Lilly in advancing healthcare through meticulous and impactful writing.
About Eli Lilly:
Eli Lilly is a global pharmaceutical company headquartered in Indianapolis, Indiana, dedicated to discovering and delivering life-changing medicines. With over 50,000 employees worldwide, the organisation focuses on complex challenges in healthcare, striving to improve the understanding and management of health while supporting the communities it serves.
Job Details:
- Designation: Associate – Medical Writing
- Category: Research & Development
- Job Type: Full Time Regular
- Job ID: R-111668
Job Description:
The purpose of the Associate, GSC Regulatory role is to work with cross-functional, multidisciplinary teams to lead the development of documents intended for regulatory audiences. This includes protocols, clinical study reports, briefing documents, regulatory responses, Investigational New Drug Applications, and marketing authorisation applications. The role requires effective project management and collaboration to ensure timely completion of high-quality regulatory documents.
Key Responsibilities:
- Effectively collect and evaluate data, information, and input from multiple sources to create a cohesive content strategy for writing projects.
- Plan, write, edit, review, coordinate, and complete regulatory documents supporting clinical development/product registration.
- Conduct effective document initiation meetings to ensure authoring team alignment.
- Ensure data are presented clearly, accurately, and concisely.
- Coordinate expert/scientific reviews and prepare final versions of documents.
- Lead the writing process and apply effective project management skills.
- Maintain and enhance therapeutic area knowledge for assigned projects.
- Provide coaching to others by sharing technical information and best practices.
Eligibility Criteria for the Medical Writing Job:
- Bachelor’s degree in a scientific, health, communications, or technology-related field.
- Demonstrated experience in technical/regulatory scientific writing.
- Strong communication and interpersonal skills.
- Successful completion of a writing exercise as part of the candidate evaluation process.
Required Skills for the Medical Writing Job:
- Graduate degree with a formal research component or in life sciences.
- Demonstrated mastery of verbal and written English skills in medical, scientific, or technical writing.
- Experience writing regulatory and clinical trial documents.
- Demonstrated project management and time management skills.
- High-level end-user computer skills (e.g., word processing, spreadsheets, presentations).
This position at Eli Lilly represents a significant opportunity for qualified candidates to contribute to impactful work in the pharmaceutical industry. Interested individuals are encouraged to apply before the deadline to be part of a mission that truly matters for patients.
