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. We're looking for people who are determined to make life better for people around the world.
The Clinical Data Analyst role is key in helping the Data and Analytic team deliver high quality data at the study and program level. The primary responsibility for this role is to integrate, automate and visualize clinical trial data by applying the newest, most innovative approaches. To do this requires an in-depth understanding of data flow, programming and clinical research data standards. Leadership and communication skills are required as well since the Clinical Data Analyst must partner with the Data Strategists, Clinical Data Managers and other key stakeholders within a study team.
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.
Develops analytic strategies and solutions for clinical trial studies that helps to ensure on-time delivery of high-quality data
Solutions consist of automating quality checks, creating re-usable reports, visualizations and dashboards by utilizing data standards
Supports multi-functional data review teams using statistical methods and state-of-the-art business intelligence tools
Works with team to ensure analytical work product is consistent from study to study where appropriate and that user experience is optimized and follows the design principles and standards established by the team
Anticipates and resolves key technical, operational or business problems that may impact the quality and delivery of clinical trial data
Supports submission, inspection and regulatory response activities
Effectively apply knowledge of applicable internal, external and regulatory requirements/expectations (MQA, CSQ, MHRA, FDA, ICH, GCP, PhRMA, Privacy knowledge, etc.) to all deliverables
Continually seek and implement means of improving processes to reduce work effort in the creation and maintenance of analytic solutions.
Represent Data and Analytics processes in multi-functional initiatives.
Thinks about the end-to-end data flow in order to manage risk to minimize impact on delivery.
Builds a diverse multi-functional and internal/external network to understand how different disciplines and approaches contribute to research and development.
Minimum Qualification Requirements:
Master's degree (or Bachelor's degree with 7 or more years of experience) in Computer Science, Engineering, Statistics, Technical Science or related field including 3 years of programming and system validation experience in the clinical, pharmaceutical, biotech, CRO or regulatory agency sectors
Other Information/Additional Preferences:
Proficient in relational database (SQL, P-SQL, T-SQL)
Knowledge and experience with statistical and data mining techniques
Knowledge of industry clinical data standards (SDTM / CDASH)
Good understanding of clinical trial process and clinical technology. Experience in managing a clinical trial from initiation through to completion is preferred
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)
Demonstrated exemplary teamwork/interpersonal skills
Demonstrated problem solving, attention to detail and result oriented behaviors in a fast-paced environment.
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 ( Lilly_Recruiting_Compliance@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.
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