CareerPlan

Sr Programmer Analyst

Hyderabad, IndiaFull-time2026-11-05 → 2026-11-10

Core

Lead programmer for moderately complex clinical trials studies, developing and validating SAS programs to transfer, combine, and analyze data across multiple systems for pharmaceutical research.

Role type

Senior IC statistical programmer (clinical trials)

Builds

Validated statistical programs, data listings, tables, and figures for clinical studies

Domain

Pharmaceutical industry + clinical trials

Required skills

SAS programming, data management across multiple systems, relational database structure, biostatistical metrics capture, quality control review, project timeline management, training and mentoring

Preferred skills

None stated

Technologies

SAS

Responsibilities

Lead programming on moderately complex studies, create/execute/maintain/validate data transfer and analysis programs, manage assignments to meet timelines, provide training and guidance to junior members, support bidding processes

Seniority

Senior, hands-on IC