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

About Vueverse

Vueverse partners with leading CROs, pharmaceutical, biotechnology, and healthcare organizations to deliver specialized Clinical Biometrics talent. We are continuously building our Clinical SAS Programmer Talent Network for current and future opportunities.

Key Responsibilities

Develop and validate SDTM datasets in accordance with CDISC standards.
Support ADaM dataset programming and validation.
Develop Safety and standard TLFs using SAS.
Perform data validation and quality control checks.
Support Define.xml, Reviewer Guides and regulatory submissions.
Develop and maintain SAS programs and reusable macros.
Collaborate with Data Management, Biostatistics, and Clinical teams.
Ensure compliance with SOPs, CDISC standards, and regulatory requirements.

Required Skills

SAS Programming
SDTM
Basic to Intermediate ADaM
CDISC Standards
TLF Programming
Define.xml
Pinnacle 21
Clinical Trial Data

Preferred Therapeutic Areas

Oncology
Immunology
Neuroscience
Cardiovascular
Rare Diseases
Vaccines

Eligibility

1–15+ years of Clinical SAS Programming experience.
Experience within CRO, Pharma or Biotech organizations.
Good understanding of SDTM, ADaM and Clinical Trial Programming.

Join our talent network and be considered for permanent, contract, remote and leadership opportunities across leading Life Sciences organizations.

Clinical SAS Programmers