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Eli Lilly and Company Label Management Apprentice - R-9470 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.At Lilly, we serve an extraordinary purpose. We make a difference for people around the global by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.The Lilly Professional Apprenticeship Program is a 12-month intensive fixed duration (FDE) professional development program during which the apprentice receives a combination of formal training, on-the-job learning, and mentoring in a key functional area to be equipped to compete for a Lilly position after successful completion of the apprenticeship.The Clinical Trial Supply Planning team is responsible for providing Investigational Product (study drug) management services for global clinical trials in all development phases, including partnering with medical teams to develop compound and study supply plans, package design, label creation, and other results required to initiate a Clinical Trial Material Request. The CTSP team also provides oversight of business processes related to on time study drug delivery at clinical trial sites. The Label Management Apprentice (LMA) will consistently and accurately build product label text that meets the needs of the study and is aligned with all applicable regulatory requirements. The LMA will provide input into supply planning activities by working with the Clinical Trial Material Manufacturing and Services (CTMMS) teams, creating label text, submitting the label request, and reviewing label proofs provided by external vendors. The LMA is also responsible for following all quality and regulatory requirements to consistently and accurately deliver IP labels on-time and with quality. Key Responsibilities: Create and submit label requests for all CTMMS-provided labels Review protocols, packaging designs and order forecasts to ensure label text accuracy and consistencySubmit, supervise, and ensure efficient completion of label requests to meet packaging order start timelines Successfully collaborate with internal/external partners Identify and execute on opportunities to improve label strategies by accelerating the timeline, reducing costs, and minimizing risks Prevent issues through planning and customer education. Proactively identify and resolve issues as the need arises. Proactively propose new phrases for addition to Lillys label phrase library Proactively identify ways to improve day-to-day activities and practices and actively communicate the opportunities to process owner(s) and leadership Collecting and reporting metrics Basic Qualifications:HS Diploma or Equivalent and 3 or more years of related or professional experience. Proven experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint) Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.Additional Skills and Preferences:At least 1 year of college and/or associate degree in a related field. Experience, knowledge and desire to work in STEM3 years experience in Clinical Trial Material Manufacturing and Services or related clinical roleExcellent interpersonal and networking skillsEffective written and verbal communication skillsAbility to work