Associate, Global Scientific Communications, Publications Medical Writer
$65.25k - $148.5kEli Lilly
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 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. Primary Responsibilities Content Strategy: 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 publication of scientific data in peer-reviewed journals and forums. Conduct effective document initiation via a kick‑off 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 reviewers’ comments, adjust content of document as required based on internal/external input, and prepare final version. Ensure and coordinate quality checks for accuracy. Steer change of timelines and content with other team members. Advocate internally and externally for appropriate authorship criteria on all applicable work products. Project and Business Partner management Lead the writing process and apply effective project management skills to ensure on time completion of high‑quality scientific publications. Build/Communicate credible writing project timelines. Anticipate and mitigate risks to delivery. Work with teams and partners to ensure smooth and on time development of documents and raise issues, as appropriate, to ensure document completion. Effectively communicate project status to business partners. Knowledge and Skills Development Maintain and enhance therapeutic area knowledge including disease state and compound(s) for assigned project(s). Maintain and enhance scientific communication skills to align with audience needs and technology/digital evolution. Exhibit flexibility in moving across document types, therapeutic areas, and compounds, depending on project assignment. Maintain and enhance knowledge of publication guidelines. Knowledge Sharing Help train 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 takeaways. Contribute to process improvements, suggesting opportunities where appropriate. Minimum Qualification Requirements Bachelor’s degree in a scientific, health, communications, health outcomes, health economics, or public health related field. Qualified applicants must be authorized to work in the United States on a full‑time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H1‑B, TN, O-1, E‑3, H1‑B1, or L-1. Other Information/Additional Preferences This position is an Indianapolis-based role with the expectation of spending a minimum of 50% of the time in the office. Successful completion of writing exercise (a writing exercise is required as part of the candidate evaluation process). Advanced degree (PhD, MD, PharmD, MA, MBBS) in science, health related field or other appropriate subject areas (economics, epidemiology, health administration, health services, pharmacoeconomics, statistics, or other relevant sciences) is preferred. Previous training and experience in disseminating results in clinical, health economics, health outcomes, health literacy, disease management, and/or population health. Extensive experience in writing, reviewing, and publishing scientific materials and the ability to appraise scientific literature and raw data critically. Strong communication and interpersonal skills. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Compensation: $65,250 - $148,500. Full‑time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). Lilly offers a comprehensive benefit program, including eligibility to participate in a company-sponsored 401(k), pension, vacation benefits, medical, dental, vision and prescription drug benefits, flexible benefits, life insurance, death benefits, certain time off and leave of absence benefits, and well‑being benefits.
- WeAreLilly
- J-18808-Ljbffr Eli Lilly
$65.25k - $148.5k
Job Overview The Scientific Communications Associate, Publications Medical Writer works with cross‑functional, multidisciplinary teams to prepare scientific publications—including abstracts, posters, manuscripts and presentations—across the entire drug development lifecycle...ScientificFull timeWork at officeFlexible hours$65.25k - $148.5k
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