Job Description

The purpose of the Quality Medical Reviewer role in Medical Affairs is to review and approve US medical (non-promotional) and promotional materials to ensure they are medically accurate and interpreted correctly based on the review of references/citations and data available The Quality Medical Reviewer is expected to provide scientific and clinical inputs while collaborating with cross-functional teams during the review and approval of content, including attending review meetings The Quality Medical Reviewer should also be aware of and ensure that all tasks are in compliance with Lillypolicies, procedures, SOPs and guidelines, and leverage different content, project, and quality management tools to increase speed and efficiency in the review and approval of promotional and medical (non-promotional) material Primary Responsibilities: This job description intends 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 supervisor regarding your actual job responsibilities and any related duties that may be required for the position Know Lillypolicies and procedures, and review promotional and medical (non-promotional) materials Thorough understanding of Lillyquality requirements and processes (i.e., CIQ and MCA requirements) and applying these guidelines consistently during the review process Verify all data values match the source documentation such as references provided, and are also consistently used throughout the document sections, charts, legends, and footnotes Verify visual representations of data accurately convey the meaning/results of the data Ensure data represents current knowledge and published scientific data Ensure information is presented in a clear, complete, accurate, and concise manner Ensure key data, statements, and conclusions are consistent across related documents, and statements and conclusions are integrated, accurate, balanced and supported by appropriate data Collaborate with cross-functional teams such as Marketing, Medical teams, etc. during the review, approval, and management of content, including attending review meetings as and when required Demonstrate working knowledge of therapeutic areas, products and disease state information, and familiarity with trial designs, rationale, and data Understand key priorities and communication strategies across therapeutic areas and/or organizational units Expertise in tools and platforms such as Veeva Vault, project planning software (e.g., Wrike, MS Project), etc. Ensure quality, speed, value, and compliance throughout the review process Understand and actively address questions related to clinical/medical/scientific content from cross-functional teams in a timely fashion Participate in the development and review of promotional and medical content in collaboration with brand teams, regulatory, copyeditors, etc. Responsible and accountable for the oversight and delivery of tasks Upholding Lilly procedures and processes Reviewing and approving materials in a timely manner Determining corrective actions to eliminate recurring issues Liaising with CIQ/MCA Lead and Operations teams in tracking and managing deviations Partner effectively with cross-functional colleagues and facilitate shared-learning forums to establish best practices and identify challenges across teams Offer scientific and medical input, and contribute to the development, review and approval of promotional and medical materials Adhere to best practices based on Lillyinternal standards Minimum Qualification Requirements: 2-4 years of experience working as a scientific/medical editor, copywriter, copyeditor, promotional and medical (non-promotional) content for publishing, marketing, communications, advertising agency, or pharmaceutical industry Must have a good understanding of scientific/medical/statistical terminologies Demonstrated initiative and ability to influence, collaborate, and work on cross-functional teams and ability to make decisions within scope of responsibility Demonstrated ability to prioritize and handle multiple concurrent tasks with strong attention to detail, critical thinking, and analytical ability Excellent written and verbal communication skills Ability to work well independently or as part of a team, within and across culturally and geographically diverse environments Experience working in a regulated industry (e.g., pharma) Additional Preferences In-depth familiarity with the US CIQ/MCA framework, procedures, processes, and tools like Veeva Vault, Wrike, etc. Experience in reviewing/writing Medical Affairs communications (slide decks, patient or HCP materials, etc.) Knowledge and experience specific to clinical pharmacology, therapeutic areas such as neuroscience, oncology, cardiovascular, immunology or endocrinology, or other medical and scientific fields Educational Requirements: Bacheloror Masterdegree in scientific, health, communications, technology health-related fields with formal research component

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