Scientific Writer – Toxicology | Eli Lilly and Company

Opportunities for a Scientific Writer – Toxicology are now open at Eli Lilly and Company, a global healthcare leader dedicated to creating life-changing medicines. If you have a strong background in life sciences and regulatory documentation, this third-party job post details an exceptional chance to join their Global Scientific Communications division in Bengaluru, India.

Role Overview

Scientific data and information represent the core assets of any premier pharmaceutical enterprise. In this role, you will collaborate with cross-functional, multidisciplinary teams to spearhead the authoring and formatting of non-clinical regulatory documents. The global team relies on precise metrics, making the position highly impactful for global drug development lifecycles.

Key Responsibilities

1. Document Preparation & Management: Plan, organize, write, and finalize non-clinical study reports and summaries. Ensure that all key scientific statements and data insights remain consistent across all regulatory submissions.

2. Regulatory Submissions Support: Author critical sections for Investigational New Drug (IND) applications and Marketing Authorization Applications (MAA). You will act as the subject-matter expert for non-clinical electronic Common Technical Document (eCTD) requirements.

3. Cross-Functional Collaboration: Coordinate submission strategies alongside ADME, Toxicology, Pathology, and Pharmacokinetics (PK/PD) scientists to ensure complete team alignment.

4. Timeline Oversight: Build and manage highly structured project timelines, ensuring high-quality documents are prepared, peer-reviewed, and finalized ahead of strict deadlines.

Also Check: Senior Scientist – Novartis

Qualifications

1. Education: A postgraduate or doctoral degree such as M.Pharm, Pharm.D, or M.Sc in Life Sciences, Biotechnology, Toxicology, Pharmacology, or a related scientific discipline.

2. Experience: Prior experience handling regulatory writing or study reports within a pharmaceutical company, biotechnology firm, or Clinical Research Organization (CRO).

3. Technical Skills: Deep familiarity with global health authority submission requirements, non-clinical drug development frameworks, and eCTD publishing standards.

4. Interpersonal Skills: Stellar project management capability, analytical agility, and excellent stakeholder management skills.