Principal Study Build Programmer

Eli Lilly and Company; Bengaluru; On-site; INR 1,200,000 - 1,600,000; Full time

Benefits offered by this job

Opportunities for professional growth

Engagement in community philanthropy

Job summary

A global healthcare leader is seeking a Principal Study Build Programmer to program and test clinical trial data collection databases. The ideal candidate will have a strong background in database programming and data mapping, as well as the ability to collaborate with cross-functional teams. This role aims to enhance the efficiency of data collection systems while ensuring compliance with regulatory standards.

Qualifications

• In-depth understanding of data technology and data flow.
• Experience in programming and testing clinical trial databases.
• Ability to lead complex projects across business units.

Responsibilities

• Program and test data collection systems for clinical trials.
• Ensure accurate and efficient delivery of data repository mappings.
• Support regulatory submission and inspection activities.

Skills

Database programming

Data mapping

Collaboration with data analytics

Knowledge of regulatory requirements

Education

Bachelor's degree in Computer Science or related field

Tools

eDC systems

Clinical data warehouse

Job description

Overview

Join to apply for the Principal Study Build Programmer role at Eli Lilly and Company.

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.

Path/Level: R3

Note: Roles are posted at the lowest level of a band, however, employees should search across all levels of the band to identify all opportunities. Employees hired on banded positions transfer at their current level, despite the level indicated on the job posting. For example, if a P2 candidate is selected for a P1-P3 banded position, the candidate will remain a P2 in the new role.

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.

Role and responsibilities

The Clinical Study Build Programmer - eDC is responsible for programming and testing clinical trial data collection databases, including the mapping, testing and normalization of data into a clinical data warehouse. This requires an in depth understanding of data technology, data flow, data standards, database programming, normalization and testing. The Clinical Study Build Programmer will collaborate with Data and Analytics colleagues such as the Clinical Data Associate, Clinical Data Manager and other key stakeholders to deliver standardized data collection methods and innovative validation solutions for use in global clinical trials.

Responsibilities

• 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
• Develop and test new ideas and/or apply 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
• Increase re-usability of forms and edits by improving the initial design
• Reduce postproduction changes change control process
• Anticipate and resolve key technical, operational or business problems that impact the Data and Analytics organization
• Interact with regulators, business partners and outside stakeholders on business issues
• Think with end to end in mind, consistently managing risk to minimize impact on delivery

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly 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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