Clinical SAS Programmer

Airvin Skills; Hyderabad, Chennai, Bengaluru; Sur place; INR 1 200 000 - 2 100 000; Plein temps

Résumé du poste

Airvin Skills is seeking a Clinical SAS Programmer to develop, validate, and maintain trial datasets using Base SAS, SAS Macros, and SAS SQL. You will generate Tables, Listings and Figures to support CSR and biostatistics, ensuring SDTM/ADaM compliance across projects.

Proficiency in SAS ODS and procedures, plus familiarity with R or Python, will help in ETL and data quality activities. Strong analytical skills and collaboration with cross-functional teams are essential for success.

Qualifications

• Master's degree in Bioinformatics, Biotechnology, Pharmacy (M.Pharm), or Life Sciences.
• Basic understanding or certification in Clinical SAS Programming; familiarity with R or Python is a plus.

Responsabilités

• Develop, validate, and maintain clinical trial datasets using Base SAS, SAS Macros, and SAS SQL.
• Generate TLFs (Tables, Listings, and Figures) to support CSR and biostatistics teams.
• Ensure CDISC SDTM and ADaM datasets compliance.
• Perform ETL on raw clinical data from various EDC platforms.
• Write and execute code to generate Edit Checks and resolve data discrepancies.
• Utilize SAS ODS and procedures like Proc SQL, Proc Freq, and Proc Means for reporting.
• Maintain compliance with ICH, GCP, and FDA 21 CFR Part 11.

Description du poste

Role & responsibilities

• Develop, validate, and maintain clinical trial datasets using Base SAS, SAS Macros, and SAS SQL.
• Generate highly accurate TLFs (Tables, Listings, and Figures) to support Clinical Study Reports (CSR) and biostatistics teams.
• Ensure strict compliance with CDISC standards, specifically focusing on the creation and validation of SDTM and ADaM datasets.
• Perform ETL (Extract, Transform, Load) activities on raw clinical data imported from various EDC (Electronic Data Capture) platforms.
• Write and execute code to generate Edit Checks, resolve data discrepancies, and implement robust data quality control procedures.
• Utilize SAS ODS and procedures like Proc SQL, Proc Freq, and Proc Means for custom reporting.
• Maintain compliance with regulatory guidelines including ICH, GCP, and FDA 21 CFR Part 11.

Preferred candidate profile

• Masters degree in Bioinformatics, Biotechnology, Pharmacy (M.Pharm), or Life Sciences.
• Basic understanding or certification in Clinical SAS Programming. Familiarity with R Programming or Python is a strong advantage.
• Strong analytical mindset with a keen interest in Clinical Data Management (CDM).
• Excellent problem-solving skills and the ability to work collaboratively in cross-functional clinical trial teams.