Mia Chen Email & Phone Number

Morrisville, Nc, Us

• Leads conversion of Classic Datavision/Clear to iEnvision Datavision/Clear and was the sole business subject matter expert on this project, fully directing the direction, strategy, and execution of the project on behalf of the VP• Works with cross-functional, multidisciplinary teams to prepare clinical trials scientific disclosures (SD)/publications and communicates to business units on internal SD strategies/tactics• Provides consultation on SD strategy and tactics and manages/executes tactics based upon strategy• Manages implementation for multiple compound-specific, SD plans• Develops and maintains publications strategy decks and metrics/dashboard for numerous programs• Drives content for SD meetings• Interacts with internal/external business partners/vendors about timelines/process• Coach/coordinate with medical writing vendors/contractors• Ensures disclosures are aligned to appropriate venues and methods of disclosing study results in a manner that is compliant with guidelines and policys• Identifies, evaluates, and resolves conflict• Ensures publications achieve balance between business needs, scientific integrity, and compliance with publication guidelines• Consults client on how to develop/execute SD plan and complete disclosure deliverables• Engages with customers, opinion leaders, patient advocacy groups, professional societies/medical associations, publishers• Builds cross-functional relationships within the company. Collaborates & advises teams on publication planning/execution for launches• Point of contact for SD plan tactics• Leads/provides clarification on local implementation of SOPs across teams/affiliates• Functions as SME for potential process improvements, industry guidelines pertaining to data dissemination, and interactions with health care providers• Works as the SME for all internal publication systems (iEnvision Datavision/Clear, Classic DV/Clear)• Manages all internal scientific communications SharePoint sites

Indianapolis, Indiana, Us

•Leads development of scientific disclosure strategy for assets/portfolio, providing effective & novel publication strategies•Engages with customers, opinion leaders, patient advocacy groups, professional societies/medical associations, & publishers•Builds close/cross-functional relationships with development/medical affairs & other experts within Lilly. Collaborates & advises teams on publication strategy/planning/execution & best practices for launches•Functions independently as decision-maker on publication-related issues•Collaborates with Alliance Management to formulate publication/disclosure charters for alliance partner products•Responsible for management/delivery of overall book of work for assigned areas•Develops & executes sourcing plans to ensure delivery of asset plan & priorities•Collaborates with functional leadership to ensure alignment of business planning/operations & develops alliances with therapeutic areas, phases of development, and geographies•Recruits/develops/retains strategic & operationally capable workforce skilled & knowledgeable in scientific communications•Effectively builds & manages organization that continuously meets the needs of changing portfolio•Develops staff who demonstrate expertise in drug development, therapeutic area, critical thinking, project management & cross-functional leadership•Provides mentoring/training/supervision & evaluates performance to direct reports/staff•Leads development of new and emerging capabilities •Functions as authority on SD strategy, planning and execution, industry standards/guidelines•Partners/designs/creates training on publication practices for audiences in/outside of GSC•Serves as a subject matter expert & represents publications on committees/task forces•In partnership with others, develops, implements, and updates Lilly publication policies, practices and tools and procedures that are compliant with industry guidelines

Indianapolis, Indiana, Us

• Works with cross-functional, multidisciplinary teams to prepare clinical trials SD/publications• Plans, writes (first-draft authoring), edits, reviews, and coordinates disclosures• Effectively collects and evaluates data/information/input from multiple sources, functions, and regions to ensure authoring team alignment/understanding• Assists in building persuasive and scientific-based arguments that support the purpose of more complex and/or strategic documents• Ensures that key data, strategically aligned scientific narrative, elements and resource documents are included appropriately, accurately, balanced and supported by appropriate data• Exhibits flexibility in moving across multiple document types and compounds• Works with teams to ensure smooth and timely development of documents and escalate issues, as appropriate, to ensure document completion and to be able to influence or negotiate change of timelines and content• Provides oversight on individual deliverables, including timeline management, delivery of feedback and issue management by building and managing relationships with vendor/alliance partners• Possess overarching view of compound/therapeutic area/external environment with ability to participate effectively in the scientific data disclosure planning, clinical planning, and/or current awareness literature updates and reviews• Networks different functions and regions to identify and contribute to process improvements, suggesting opportunities where appropriate

Indianapolis, Indiana, Us

• Develops and characterizes novel biomarker assays using techniques such as IHC/ISH for pre-clinical research and to support clinical trial assay development efforts• Serves as expert on multiple techniques/equipment platforms• Support Lilly’s NGR efforts by implementing the BaseScope assay in the DEP lab for direct application to “Trailblazer” projects that had portfolio impacts• Leads and manages multiple high priority projects• Contributes to project design/protocol/technique/process/SOP development and improvement

Cincinnati, Oh, Us

• Supports the histology group by processing, embedding, staining, and tracking human and mouse tissue/samples• Establishes and maintains human cancer cell lines to use for portfolio research projects

Indianapolis, In, Us

• Responsible for an independent project looking at how Kinase suppressor of Ras modulates mast cell function and its relations to inflammatory diseases and oncology related pathways (project design and execution)• Looks at how the deletion of Vav1 affects mast cell functions• Develops expertise in laboratory techniques, analysis, presentations, and publications

Master Of Business Administration - Mba (Expected 2024)

Master Of Science (M.S.), Biology

Biology Bs, Biology, Chinese, Animal Behavior