Tata Consultancy Services (TCS) is a globally renowned IT services, consulting, and business solutions organization that has been helping clients across industries achieve digital transformation. As a pioneer in IT services, TCS operates in over 46 countries, delivering innovative solutions and fostering a collaborative work environment. With a strong presence in the healthcare and pharmaceutical sectors, TCS offers opportunities for talented professionals to drive impactful projects and enhance their careers.
Job Responsibilities
As a Clinical SAS Programmer at TCS, your primary role will involve developing and validating statistical programming deliverables for clinical studies. Key responsibilities include:
- SAS Programming: Develop SAS® programs for datasets, tables, listings, and figures (TLFs) as assigned by the Lead Statistical Programmer.
- Validation and Quality Assurance: Perform quality checks and validation of datasets and outputs to ensure accuracy and compliance.
- Documentation: Prepare data derivation specifications following standard guidelines and maintain an understanding of study documentation.
- Adherence to Standards: Ensure compliance with ICH-GCP guidelines, core operating procedures, and work instructions.
- Macro Development: Develop study-level macros under the direction of the Lead Statistical Programmer to streamline programming tasks.
- Timeline Management: Track deliverables, monitor status using trackers, and ensure timelines are met.
- Issue Resolution: Identify, track, and escalate unresolved issues appropriately to the Lead Statistical Programmer for resolution.
- Collaboration: Work closely with clinical data managers, statisticians, and cross-functional teams to support project goals.
Qualifications
To be considered for the Clinical SAS Programmer role, candidates should meet the following qualifications:
- Bachelor’s or Master’s degree in Pharmaceutical Sciences, Life Sciences, Statistics, Mathematics, or Computer Science.
- Strong understanding of clinical trial data, statistical programming, and data management principles.
- Experience in SAS programming and statistical software for clinical trials is preferred.
Key Skills
The ideal candidate will possess the following skills:
- Proficiency in SAS® programming, including Base SAS, SAS/STAT, and SAS/Macro.
- Experience with clinical trial datasets (SDTM, ADaM) and TLF development.
- Strong understanding of ICH-GCP guidelines and regulatory requirements.
- Excellent problem-solving and analytical skills.
- Attention to detail and the ability to maintain high-quality deliverables.
- Effective communication and team collaboration skills.
- Ability to manage multiple tasks and meet tight deadlines.
