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Eli Lilly and Company Clinical Laboratory Sciences Associate - R-9567 in Indianapolis, Indiana

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 39,000 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. Were looking for people who are determined to make life better for people around the world.Purpose: The TA Associate, Clinical Laboratory Sciences will have early engagement with the appropriate study team, business and therapeutic partners on development of the clinical laboratory, diagnostic and biomarker strategies at the trial level. The TA associate coordinates vendor activities for assigned trials as well as facilitates research and resolves any clinical laboratory and diagnostic issues or needs throughout the life of the trial. They partner with the clinical team to provide input into the protocol development/design, develop and implement the integrated trial clinical laboratory plans and the review and monitoring of resultant data, ultimately providing high quality, combinable data in a cost effective and efficient fashion.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. Portfolio Strategy, Planning and Delivery:Provide clinical and diagnostics support, expertise and consultation on biomarkers (including assay development and validation), as well as oversight of all clinical laboratory, ECG, imaging, sample storage and other clinical diagnostic technical and logistical needs for assigned trial(s)Provide input and review of the protocol related to clinical laboratory and diagnostic needsProvide and coordinate clinical testing plans and study risk oversight as it pertains to clinical labs, diagnostic data reviews, and lab management plansPartner with the Sourcing organization to follow the proper sourcing strategy for vendor assignment2. Project Management :Raise issues as warranted to upper managementProactively monitor for issues and trendsDrive clinical laboratory data completeness and accuracy within business systemsDrive communications to prospectively manage upcoming cross-functional activities, key deliverables and decisions as well as to proactively identify updates to schedule and partner with clinical to optimize timelineArticulate the value of clinical laboratory solutions in terms of reliability, time, cost, quality and scalabilityMonitor trial budgets and ensure FRAP complianceMaintain accurate budget information and defined protocol testing in the Laboratory and Diagnostic toolMaintain inspection readiness at all times by maintaining a complete eTMF at a trial levelKeep study team abreast of trial specific metrics and issues3. People Development Engage fully in the performance management processModel the Lilly core values and behaviorsProvide peer coaching within the organization that champions inclusion and innovation, process improvement, and an external awareness and understandingMinimum Qualification Requirements:Bachelors degree in a science or related life science fieldOther Information/Additional Preferences:Education or experience in Nursing, Medical technology, biology, chemistry is highly preferredKnowledge of clinical drug developmentPrior laboratory experience or knowledge of laboratory testingStrong self-management skillsStrong team ethic and interpersonal skillsStrong communication skills (verbal and written)Conceptual understanding of information technologyStro