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Lilly Clinical Data Analyst Intern-Fulltime 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 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.

Purpose:

The Clinical Data Analyst is responsible for programming and testing clinical data reports, dashboards and analytics in a manner that allows for seamless downstream consumption, standardization, and integration of data. This requires an in depth understanding of end-to-end data programming, testing, data technology, data flow, and data standards. The Clinical Data Analyst collaborates with the Clinical Data Strategist, Clinical Data Lead, Clinical Data Management Associate, Clinical Data Associate, and other key stakeholders to deliver standardized reports, dashboards and innovative analytic solutions for use in global clinical trials.

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.

Portfolio Delivery

  • Program and test data reporting, dashboarding and analytics for a trial or set of trials within a program using data standards library

  • Ensure data reporting and analytics are delivered accurately, efficiently and in alignment with study objectives

  • Provide insights into study level deliverables (i.e., Data Management Plan, Project Plan, database, and observed datasets)

  • Support submission, inspection, and regulatory response activities

  • Lead large-scale cross Business Unit/Therapeutic Area projects or programs with high complexity

  • Develops and tests new ideas and/or applies innovative solutions that create value to the portfolio

  • Independently identifies key scientific questions/issues and develops solutions to advance the portfolio

Project Management

  • Increase speed, accuracy, and consistency in the development of reporting and analytic capabilities and deliverables

  • Partner with Clinical Data Management Associate and Data Strategist to deliver data reporting and analytics per business need

  • Comply with and influence data standard decisions and strategies for a study and/or program

  • Utilize therapeutic knowledge and possess a deep and broad understanding of the technology to develop data reports and analytic solutions

  • Effectively apply knowledge of applicable internal, external, and regulatory requirements/expectations (MQA, CSQ, MHRA, FDA, ICH, GCP, PhRMA, Privacy knowledge, etc.) to all deliverables

  • Integrates cross-functional and/or external information and applies technical knowledge to data-driven decision making

Enterprise Leadership

  • Continually seek and implement means of improving processes to reduce data reporting/analytics and decrease work effort Represent Data and Analytics processes in cross-functional initiatives

  • Actively participate in shared learning across Data and Analytics organization

  • Work to Increase re-usability of reports and analytics

  • Work to enable automation and seamless data delivery with real time data validation

  • Anticipate and resolve key technical, operational or business problems that impact the Data and Analytics organization

  • Interacts with regulators, business partners and outside stakeholders on business issues

  • Thinks with end to end in mind consistently managing risk to minimize impact on delivery

  • Builds a diverse cross-functional and internal/external network to understand how different disciplines and approaches contribute to research and development

  • Focuses on defining analytic solutions to answer scientific questions, goals, critical success factors and timelines in support of advancing the portfolio

Minimum Qualifications and Requirements

  • Master’s degree (or bachelor’s degree with equivalent experience) in Computer Science, Engineering, Statistics, or related field graduating by August 2022.

  • Must have completed a previous internship with Eli Lilly

Other Information/Additional Preferences

  • Technical knowledge to develop requirements and/or study project deliverables

  • Knowledge and experience with statistical techniques

  • Programming languages - Industry tools and languages like Tableau, PowerBI, Python, SAS, ‘R’ and Shiny for reporting, metrics and visualizations along with P-SQL, T-SQL for DBMS.

  • Proven ability to work creatively and analytically in a problem-solving environment

  • Quick learner to new trends in technology

  • Excellent leadership, communication (written and oral) and interpersonal skills

  • Demonstrated leadership

  • Demonstrated teamwork and collaboration

  • Exposure to Python and Power BI

  • Experience with the following: o Articulating the flow of data (structure and format) from patient to analysis and apply this knowledge to data solutions o Utilization of clinical/drug development knowledge and an ability to liaise effectively with study team members (i.e. Data Sciences, Statistics, PK, Operations, Medical) o Strong therapeutic/scientific knowledge in the field of research

  • Society of Clinical Data Management certification

  • Project management experience

  • Familiarity with clinical data tools and technologies

  • Understanding and experience in using data standards

  • Knowledge of medical terminology

  • Passionate about improving technological solutions using new technologies

  • Domestic and International travel may be required

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.

As a condition of employment with Eli Lilly and Company in the United States and Puerto Rico, you must be fully COVID-19 vaccinated and provide valid proof of vaccination to the company.

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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