Description:
• Develop, validate, and maintain statistical programs in SAS for Tables, Listings, and Figures (TLFs).
• Perform data manipulation, analysis, and visualization using R and SAS with relevant packages.
• Collaborate with biostatisticians and data management teams to support clinical study deliverables.
• Ensure compliance with regulatory standards and company SOPs.
• Conduct quality control and validation of programming outputs.
• Support submission activities and related documentation as needed.
Requirements:
• Bachelor’s or Master’s degree in Statistics, Biostatistics, Computer Science, or a related field.
• 3+ years of experience in statistical programming within the pharmaceutical or biotech industry.
• Hands-on experience with R programming in a clinical trial environment.
• Good understanding of R packages.
• Good understanding of CDISC standards, including SDTM and ADaM.
• Strong knowledge of clinical trial data and regulatory requirements.
• Experience working in an FSP model or with global pharmaceutical clients is preferred.
• Exposure to submission activities such as FDA/EMA submissions is preferred.
• Familiarity with SAS alongside R is a plus.
• Strong problem-solving and communication skills.
Benefits:
• Permanent position with ClinChoice.
• Opportunity to work directly for a single sponsor while benefiting from a global CRO environment.
• Remote work designation (#LI-Remote).
• Opportunity to join a global company with 4,000+ professionals across 20+ countries.
• Continuous training and development support.
• Equal opportunity employer with a diversity- and inclusion-focused culture.