Experience: 1–15+ Years
Location: PAN India | Hybrid | Remote | On-site

About Vueverse

Vueverse partners with global CROs, pharmaceutical and biotechnology companies to support Statistical Programming requirements across all phases of clinical development. We are building a strong Statistical Programmer Talent Network for current and future opportunities.

Key Responsibilities

Develop and validate ADaM datasets in accordance with CDISC standards.
Program and validate Safety and Efficacy Tables, Listings and Figures (TLFs).
Implement Statistical Analysis Plans (SAPs).
Perform independent programming validation and quality control.
Develop SAS programs and reusable macros.
Support regulatory submissions including Define.xml and Reviewer Guides.
Collaborate closely with Biostatisticians and cross-functional study teams.
Support integrated analyses (ISS/ISE) where applicable.

Required Skills

Advanced SAS Programming
ADaM
TLF Programming
CDISC Standards
Statistical Analysis Plans (SAP)
Validation & QC
SAS Macros
Define.xml
Pinnacle 21
R Programming (Preferred)

Preferred Therapeutic Areas

Oncology
Immunology
Neuroscience
Cardiovascular
Rare Diseases

Eligibility

1–15+ years of Statistical Programming experience.
Experience in ADaM, TLF Programming and Clinical Trial Reporting.
Ability to work independently with Biostatisticians and Study Teams.

Join our Statistical Programming Talent Network and gain access to exciting opportunities with leading Life Sciences organizations.