Senior Statistical Programmer (SAS Clinical Programming)

About the Company

Greetings from Teamware Solutions a division of Quantum Leap Consulting Pvt. Ltd

Teamware Solutions (a division of Quantum Leap Consulting Pvt. Ltd.) is a 20+ year industry leader providing IT staffing and consulting services, supporting 4000+ professionals across India, the USA, the Middle East, and APAC for leading GCC clients.

About the Role

We are hiringa Senior Statistical Programmer (SAS Clinical Programming)

• Location: Bangalore
• Work Model: Onsite
• Experience: 4-8 years
• Notice Period: Immediate - 15 days

Senior Statistical Programmer | SAS | CDISC (SDTM/ADaM) | TLF

We are hiring for two exciting opportunities with a leading global pharmaceutical client.

1. Senior Statistical Programmer 1 (4-6 years of experience

2. Senior Statistical Programmer 2 (6-8 years of experience)

Statistical Programming Services

Key Responsibilities

• Develop SAS programs for analysis datasets, tables, listings, and figures (TLFs).
• Validate programming outputs and ensure high-quality deliverables.
• Support statistical analysis, programming strategies, and regulatory submissions.
• Review analysis plans and assess programming requirements.
• Collaborate with project teams and external vendors.
• Ensure compliance with CDISC standards, regulatory guidelines, and SOPs.
• Independently deliver programming assignments and support process improvements.

Skills, Knowledge, and Experience

Minimum Requirements:

• Bachelor's degree in statistics, biostatistics, mathematics, computer science or life sciences required.

• At least 8 years programming experience in clinical industry recommended.

• Demonstrated proficiency in analytical programming

• Have in-depth understanding of clinical data structure (e.g. CDISC standards) and relational database.

• Demonstrated skills in using software tools and applications, e.g., MS office, XML, Pinnacle 21.

• Demonstrated ability in the handling and processing of upstream data, e.g., multiple data forms, workflow, eDC, SDTM.

• Demonstrated ability in providing outputs to meet downstream requirements, e.g., ADaM, Data Definition Table, e-submission.

• Have good understanding of regulatory, industry, and technology standards and requirements.

• Have good knowledge of statistical terminology, clinical tests, medical terminology and protocol designs.

• Demonstrated ability to work in a team environment with clinical team members.

Preferred Requirements:

• Minimum of 10 years clinical / statistical programming experience within pharmaceutical clinical development - Supporting regulatory filings (e.g. NDA, BLA, MAA)

• Knowledge of the drug development process, clinical trial methodology, statistics and familiarity with global regulatory requirements

• Experience in other software packages (e.g. R)

• Experience with the Linux operating system

Please let me know if you are interested in this position and send me your resume to [Confidential Information]