eCOA Clinical Study Programmer — Build & Validate Data

Eli Lilly and Company; Indiana (PA); On-site; USD 80,000 - 169,000; Full time

Job summary

Eli Lilly and Company in Indianapolis, Indiana, seeks a Clinical Study Build Programmer - eCOA to design, program and validate clinical data collection databases, map data to a common warehouse, and ensure accurate data delivery across global trials.

You will collaborate with Data & Analytics colleagues and study teams to implement standardized methods and innovative validation solutions for real-world studies.

Qualifications

• Master’s degree in a scientific field such as Informatics/Analytics, Life Sciences, Statistics, Information Technology, Epidemiology, Computer Sciences.
• +3 years of related experience in clinical data management or areas closely intersecting with clinical data management.

Responsibilities

• Programming and configuring clinical data collection systems (eCOA/EDC platforms).
• Study build programming including form logic, edit checks and workflows.
• Map data collection systems and data warehouse mappings for trials.
• Influence eCOA design specifications and enable localization.
• Ensure data collection systems align with study objectives and regulatory expectations.
• Support submission, inspection and regulatory response activities.
• Lead cross-BU/TA projects with high complexity.

Education

Master’s degree in a scientific field

Tools

eCOA platforms

EDC platforms

Job description

Eli Lilly and Company in Indianapolis, Indiana, seeks a Clinical Study Build Programmer - eCOA to design, program and validate clinical data collection databases, map data to a common warehouse, and ensure accurate data delivery across global trials.

You will collaborate with Data & Analytics colleagues and study teams to implement standardized methods and innovative validation solutions for real-world studies.