Senior SAS Programmer

• Lead SAS programming activities for clinical studies, ensuring adherence to study protocols, statistical analysis plans (SAPs), and regulatory requirements.
• Develop, validate, and maintain SAS programs to generate analysis datasets, TLFs, and other clinical trial deliverables.
• Collaborate closely with cross-functional teams including statisticians, data managers, and clinical operations to ensure timely and accurate deliverables.
• Provide technical guidance and mentorship to junior programmers, ensuring adherence to programming standards and best practices.
• Participate in study team meetings, contributing SAS programming expertise to study design and analysis strategies.
• Contribute to the development and implementation of departmental programming standards and processes to optimize efficiency and ensure quality.
• Ensure compliance with regulatory guidelines (e.g., FDA, ICH) and company SOPs throughout all programming activities.

• Bachelor's degree in Computer Science, Statistics, Mathematics, or a related field; advanced degree preferred.
• Hands-on experience in SAS programming within the pharmaceutical, biotechnology, or clinical research industry.
• Proficiency in SAS/Base, SAS/STAT, SAS/Macro, and other relevant SAS modules.
• Demonstrated experience in leading SAS programming efforts for clinical studies, including complex TLFs.
• Strong understanding of CDISC standards (e.g., SDTM, ADaM) and their application in clinical trials.
• Excellent problem-solving skills, attention to detail, and ability to work effectively in a team environment.
• Proven ability to effectively communicate technical concepts to non-technical stakeholders.
• Experience with submission deliverables and familiarity with regulatory requirements (e.g., FDA, EMA) preferred.
• Prior experience in mentoring junior programmers and leading programming teams is desirable.