Job Summary
We are seeking a skilled Statistical Programmer with over 5 years of experience in clinical/statistical programming and at least 1 year of hands-on experience in R programming. The ideal candidate will be responsible for developing, validating, and maintaining statistical programs to support clinical trials and data analysis.
Key Responsibilities
- Develop and maintain statistical programming deliverables using R and/or SAS.
- Perform data manipulation, analysis, and reporting using R programming.
- Generate tables, listings, and figures (TLFs) for clinical study reports.
- Ensure quality and accuracy of outputs through validation and adherence to standards.
- Work with cross-functional teams including biostatistics, data management, and clinical teams.
- Follow CDISC standards such as SDTM and ADaM where applicable.
- Support regulatory submissions by preparing compliant datasets and documentation.
- Optimize and automate workflows using R scripts and reusable functions.
Required Skills & Qualifications
- Bachelor's or Master's degree in Statistics, Mathematics, Life Sciences, or related field.
- 5+ years of experience in statistical programming.
- Minimum 1 year of hands-on experience in R (mandatory).
- Strong knowledge of statistical programming concepts and data handling.
- Experience with clinical trial data and regulatory requirements is preferred.
- Good understanding of CDISC standards (SDTM, ADaM).
- Strong problem-solving and analytical skills.
- Excellent communication and teamwork abilities.
