Statistical Programmer, Consultative COA Scoring
IQVIA (company site, opens in a new tab)BengaluruOn-siteDirect career pageEst. 10–20 LPA
Posted 18h ago
Reach people at IQVIA
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 IQVIA 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
- Develop scoring rules and algorithms for existing clinical outcome assessment (COA) measures, including scoring documentation, simulation datasets, data-quality evaluation and domain scoring.
- Program statistical and psychometric analyses for new COA measures and endpoints, including meaningful-threshold analyses and work with high-frequency or continuous digital health technology (DHT) data.
- Build statistical features for internal tools and support validation of digital measures with data scientists, working across patient-centered research teams.
Minimum Requirements
- Work Experience Required: Experience in statistical programming; duration not specified.
- Relevant qualification in statistics or psychometrics.
- Statistical and psychometric research skills, plus strong computer skills including Base SAS with macros; R skills and API experience are also listed.
- Extensive familiarity with AI tools and their application to the relevant topics.
Ideal Candidate Profile
- Has experience applying statistical programming and psychometrics to COAs, patient-centered research, DHTs, or clinical research in pharmaceutical or healthcare settings.
- Can work across measure development, scoring, simulation and validation, translating statistical methods into documented algorithms and usable tools.
- Experience with regulated-environment programming and validation/QC, database connections using SAS or R, or pharmaceutical consulting would be an advantage.