Lilly Hiring for Associate/Senior Associate Manager – Narrative Writer at Bengaluru, India Full Time

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.

Global Scientific Communications (GSC) Scientific Communications Associate – Regulatory Position title/level may vary by site or geographic location Purpose: Scientific data and information are core assets of Lilly. Providing balanced, objective, and accurate information to regulators, the scientific community, health care professionals, payers, and patients in a consistent and timely fashion across the entire drug development lifecycle is fundamental to Lilly. The purpose of the Scientific Communications Associate – Regulatory role is to work with cross-functional, multidisciplinary teams to lead the development of documents intended for regulatory audiences (including, but not limited to, clinical study reports, briefing documents, regulatory responses, Investigational New Drug Applications, and marketing authorization applications).

Primary Responsibilities: This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.

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.

1. 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.

1. Knowledge and Skills Development

• Maintain and enhance therapeutic area knowledge including disease state and compound(s) for assigned project(s).

• Exhibit flexibility in moving across document types, therapeutic areas, and compounds, depending on project assignment.

• Maintain and enhance knowledge of regulatory guidelines and publication guidelines.

• Possess overarching view of compound, therapeutic area, and external environment (including competitors) with ability to participate effectively in clinical planning, submission strategy planning, customer regulatory responses, and/or current awareness literature updates and reviews.

• Maintain and enhance the scientific communications skills to align with the audience needs and with the changes in technology and platforms.

1. Knowledge Sharing

• Provide coaching to others by sharing technical information, giving guidance, answering questions.

• Recognized for technical expertise in specific document development.

• Network with others (including other functions and regions) to identify and share best practices.

• Contribute to process improvements, suggesting opportunities where appropriate.

• Provide database and other tool (e.g., document management systems) expertise.

Minimum Qualification Requirements:

• 3-10 years’ experience as a narrative writer (specific to clinical study report submission) or combined exp of regulatory/ narrative writer

• Ability to lead/manage submission projects independently

▪ 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)

Other Information/Additional Preferences:

• Experience with tool/technology

▪ 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

▪ Experience in clinical development, clinical trial process or regulatory activities.

▪ Demonstrated project management and time management skills.

▪ Demonstrated high-level end-user computer skills (e.g., word processing, tables and graphics, spreadsheets, presentation and templates).

Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( LillyRecruitingCompliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

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!

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