Deskripsi Pekerjaan
Join IQVIA as a Senior Statistical Programmer and become a key player in transforming healthcare data into meaningful insights. In this critical role, you'll be responsible for developing, testing, and validating statistical programming solutions that support clinical trials and research studies. Your expertise will directly contribute to the advancement of medical treatments and improve patient outcomes worldwide.
As a Senior Statistical Programmer at IQVIA, you'll work with cutting-edge technologies and methodologies to analyze complex datasets, create statistical reports, and ensure data integrity throughout the clinical trial process. You'll collaborate with cross-functional teams including biostatisticians, clinical research associates, and data management specialists to deliver high-quality programming solutions that meet regulatory standards.
This position offers an exceptional opportunity to grow your career in a dynamic environment where innovation is valued, and your contributions make a tangible impact on global healthcare. If you're passionate about statistics, programming, and making a difference in healthcare, IQVIA is the perfect place to advance your career.
Tanggung Jawab
- Develop, test, and validate statistical programming solutions for clinical trials and research studies
- Create, maintain, and document SAS programs for data analysis, reporting, and presentation
- Collaborate with biostatisticians and clinical research teams to understand programming requirements
- Ensure data integrity and quality through rigorous programming validation and verification processes
- Generate statistical tables, listings, and figures for regulatory submissions and clinical reports
- Maintain compliance with regulatory guidelines and industry standards for statistical programming
Kualifikasi
- Bachelor's or Master's degree in Computer Science, Mathematics, Statistics, Life Sciences, or related field
- Minimum 3-5 years of experience in statistical programming, preferably in a clinical research environment
- Proficiency in SAS programming with strong knowledge of SAS macro language and advanced SAS procedures
- Experience with CDISC standards (SDTM, ADaM) and clinical trial data management systems
- Strong problem-solving skills and attention to detail with the ability to work independently and as part of a team
- Excellent communication skills with the ability to effectively present complex technical information