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Lilly Imaging Data Associate in Philadelphia, Pennsylvania

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 35,000 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. We’re looking for people who are determined to make life better for people around the world.

Avid Radiopharmaceuticals, Inc. (Avid RP), a wholly-owned subsidiary of Eli Lilly and Company, is a molecular imaging company developing diagnostics and biomarkers that improve global health by accelerating the development of new medicines and enabling a tailored approach to healthcare. For more information, visit www.avidrp.com .

Position Overview:

The Imaging Data Associate is responsible for working independently to ensure imaging data is managed efficiently between internal and external parties. They are responsible for implementing improvements for imaging data organization and management processes (e.g., scripting and programming support, batch processing and transfer of image files, interface build between EDC and image files to allow for sorting of scans, syncing with external database or PACS systems, etc). The Data Associate will learn imaging systems, implement new workflows, support system upgrades and user acceptance testing.

Responsibilities:

  • Create efficiencies and file management within the Lilly IT infrastructure and well as within imaging software systems through scripting and advanced file handling

  • Manage automated image and data file transport between internal and external systems in accordance with applicable standard operating procedures (SOPs) using tracking tools on Avid systems

  • Interface between EDC and image files to accommodate specific requests from internal and external partners

  • Creation of systems to allow controlled access to imaging data (including intermediate analysis files) across organization

  • Perform PET image analysis utilizing appropriate, validated pipelines

  • Support development and validation of iPACS activities

  • Perform phantom analysis for clinical trial qualifications

  • Maintain and track imaging-related files in electronic software systems

  • Assist with storing all imaging documentation for imaging site files and the trial master file

  • Collect and analyze findings on images and present results to independent reviewer and/or medical review staff

  • Author documentation pertaining to SOPs, as well as project-specific procedures including Imaging Management Plan and Site Manual

  • Monitor within assigned projects of Good Clinical Practices (GCP), additional regulatory requirements (21CFR Part 11), applicable departmental and company-wide SOPs, and project specific protocol compliance

  • Perform other duties as assigned

Basic Qualifications

  • Bachelor's degree

Additional Skills/Preferences:

  • Minimum 2 years of experience in clinical research or imaging related field preferred

  • Experience with database applications and imaging software

  • Familiarity with image handling based on standard DICOM tags

  • Strong computer skills (Office applications, imaging software) and ability to develop additional computer skills to support image management

  • Ability to manage multiple and competing priorities through effective organization, people, and time management skills

  • Ability to manage projects

  • Excellent written and oral communication skills

  • Understanding of Good Clinical Practice

  • Excellent analytical and problem-solving skills

  • Demonstrated ability to work independently and manage multiple priorities

Additional Information:

  • Lilly currently anticipates that the base salary for this position could range from between $58,000 to $113,500 and will depend, in part, on the successful candidate’s qualifications for the role, including education and experience. Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Of course, the compensation described above is subject to change and could be higher or lower than the range described above. Further, Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( LillyRecruitingCompliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.

Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people.​ We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe!

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