What You Will Be Doing:

- Assisting in the development, validation, and maintenance of statistical programs (SAS, R, or similar) for data manipulation and analysis in clinical trials.
- Collaborating with senior statistical programmers and biostatisticians to understand project requirements and contribute to statistical analysis plans (SAPs).
- Performing data cleaning and preparation tasks to ensure data integrity and accuracy prior to analysis.
- Participating in the preparation of reports and documentation to support regulatory submissions and clinical study reports.
- Learning and applying industry standards, including ICH/GCP guidelines, to programming tasks to ensure compliance.

Your Profile:

- Bachelor s degree in statistics, mathematics, computer science, or a related field.




- Basic knowledge of statistical programming languages such as SAS or R; coursework or internships in programming is a plus.
- Strong analytical and problem-solving skills, with attention to detail and a willingness to learn.
- Ability to work collaboratively in a team setting and communicate effectively with team members.
- Familiarity with clinical trials and data management processes is an advantage but not required.

Skills: team environments , Programming Language, Clinical Trials, Data Management, Integrity

Experience: 2.00-3.00 Years

📌 Statistical Programmer I (Thiruvananthapuram)
🏢 ICON
📍 Thiruvananthapuram