eCOA Build Programmer
Eli Lilly and Company (company site, opens in a new tab)BengaluruOn-siteDirect career pageEst. 12–22 LPA
Posted 10h ago
Reach people at Eli Lilly and Company
People at this company you can reach
Log in to see who works here
Create a free account or log in to see the people at Eli Lilly and Company you could write to:
- Recruiters & HR
- People in this function
- Work addresses
Your match
Against your primary resume
Log in to see your match score
Create a free account or log in to unlock your CV match score across:
- Role fit
- Experience
- Industry relevance
Protocol Intelligence
How competitive this role is
Competition
Background fit
Strictness
Log in to see why each signal reads the way it does.
Job description
Structured overview of role & requirements
About This Role
- Design, program, and test clinical trial data collection databases (eCOA) and map data into clinical data warehouses.
- Collaborate with cross-functional teams to deliver standardized data collection methods and support regulatory activities.
- Lead complex projects to improve data integration, speed, accuracy, and consistency in clinical trial systems development.
Minimum Requirements
- Bachelor’s or Master’s degree in computer science, engineering, medical field, Informatics, Life Sciences, Statistics, Information Technology, or related with relevant experience.
- Experience in eCOA, eDC, eSource, or Direct Data Capture implementations in clinical or pharmaceutical sectors.
- Strong understanding of clinical protocols, data standards, clinical terminologies, and database programming/testing.
- Work Experience Required: Not explicitly mentioned in the JD.
Ideal Candidate Profile
- Experienced in clinical trial data systems implementation with understanding of clinical trial workflows and therapeutic knowledge.
- Ability to lead cross-business unit projects and manage vendor partnerships within pharmaceutical or biotech environments.
- Demonstrated proficiency in data technologies, project management, and applying regulatory requirements in clinical data build activities.