Work as Study Build Programmer at Lilly - Life Sciences Apply

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.

Post : Principal/Sr. Principal - Study Build Programmer

Job Description
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 collection systems and associated data repository mappings for a trial or set of trials within a program using data standards library components
• Ensure data collection systems and data warehouse mappings 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 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

Project Management
• Increase speed, accuracy, and consistency in the development of systems solutions
• Enable metrics reporting of study development timelines and pre and postproduction changes to database
• Partner with Data and Analytics colleagues such as the Clinical Data Associate, Clinical Data Management Associate to deliver study database per business need and before first patient visit
• Comply with and influence data standard decisions and strategies for a study and/or program
• Utilize therapeutic knowledge and possess a deep understanding of the technology used to collect clinical trial data
• Effectively apply knowledge of applicable internal, external and regulatory requirements/expectations (MQA, CSQ, MHRA, FDA, ICH, GCP, PhRMA, Privacy knowledge, etc.) to study build 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 study build cycle time, decrease work effort and enable the normalization of various sources of data into a common data repository in a way that allows for improved integration, consumption and downstream analysis
• 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 forms and edits by improving the initial design
• Work to reduce postproduction changes change control process
• 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

Candidate Profile
• Master’s degree in a scientific or technical field such as Informatics/Analytics, Life Sciences, Information Technology, Computer Sciences (or bachelor’s degree plus 3 or more years of experience in clinical data management, database programming or system validation experience in the clinical, pharmaceutical, biotech, CRO or regulatory agency sectors)
• 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
• Domestic and International travel may be required

Other Information / Additional Preferences :
• Experience with the following :
• Articulating the flow of data (structure and format) from patient to analysis and apply this knowledge to data solutions
• Deciding the technology platform (system/database) for data acquisition and aggregation
• Utilization of clinical/drug development knowledge and an ability to liaise effectively with study team members (i.e. Data Sciences, Statistics, PK, Operations, Medical)
• Strong therapeutic/scientific knowledge in the field of research
• Society of Clinical Data Management certification
• Project management experience
• Vendor management experience
• Familiarity with clinical data tools and technologies
• Understanding and experience in using data standards
• Experience with designing and handling of eCOA data
• Knowledge of medical terminology

Additional Information
Qualification : Master’s degree
Location : Bangalore, Karnataka
Industry Type : Pharma/ Healthcare/ Clinical research
Job ID : R-91692
End Date : 15th October 2025