Job Title : Sr. SAS Programmer

Location : Hyderabad/Bangalore/Chennai/Pune

Work Mode : Work from Office (5 days a week)

Job Type : Full time

Essential Duties and Responsibilities :

As a Sr. SAS Programmer, you will be creating, validating, and maintaining statistical programs and datasets used in regulatory submissions.

Key Responsibilities :

Develop and validate SAS Macro's/programs for :

- Data cleaning and transformation

- Analysis datasets (ADaM)

- SDTM datasets (Study Data Tabulation Model)

- Generate Tables, Listings, and Figures (TLFs)

- Ensure compliance with CDISC standards (SDTM, ADaM) & Regulatory guidelines (FDA, EMA)

- Perform quality checks and validation of outputs

- Collaborate with other stakeholders like Biostatisticians & Clinical data management teams

- Support submission packages for regulatory authorities

Required Skills :

- Strong proficiency in Base SAS, SAS/STAT, SAS Macros

- Experience with CDISC standards (SDTM & ADaM)

- Knowledge of Clinical trial processes & Good Clinical Practice (GCP)

- Familiarity with Regulatory submissions (eCTD)

- Good analytical and problem-solving skills

Qualifications :

- Bachelors or Masters degree in Statistics / Biostatistics, Computer Science or Life Sciences

- Typically 5 - 12 years of SAS programming experience (varies by level)

Preferred Qualifications :

- Experience in pharmaceutical or CRO industry

- Exposure to tools like SAS, R & Python

- Prior work on submission projects