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 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 Analytics Associate is responsible for programming and testing clinical trial data reports, dashboards and analytics. This requires an in depth understanding of data programming, testing, data technology, data flow, and data standards. The Clinical Data Analytics Associate collaborates with the Clinical Data Management Associate, Clinical Data Associate and other key stakeholders to deliver standardized reports, dashboards and innovative analytics 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
Project Management
Increase speed, accuracy, and consistency in the development of reporting and analytic capabilities and deliverables
Partner with Clinical Data Management Associate to deliver data reporting and analytics per business need
Comply with data standard decisions and strategies for a study and/or program
Utilize therapeutic knowledge and possess a deep understanding of the technology to develop data reports and analytics
Effectively apply knowledge of applicable internal, external, and regulatory requirements/expectations (MQA, CSQ, MHRA, FDA, ICH, GCP, PhRMA, Privacy knowledge, etc.) to all deliverables
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
Minimum Qualification Requirements:
Minimum Bachelor's degree in Computer Science, Engineering, Statistics, Technical Science, or related field with 3-5 years of clinical experience in a pharmaceutical, biotech, CRO, or Regulatory agency.
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 in professional setting.
Demonstrated teamwork and collaboration in a professional setting.
Job located in Bangalore, India
Preferred skills:
Clinical background with substantial experience in data reporting using
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