Develop and test SAS and/or Python programs to generate standard and non-standard clinical data files
Review and interpret data specifications, collaborating with Data Management to finalize requirements
Support the validation of encoding and programming outputs to ensure accuracy and compliance
Process data extracts and manage daily encoding requests to support ongoing study activities
Contribute to study archival processes and ensure data deliverables meet project timelines
Perform ad-hoc programming and data analysis activities, including quality control checks, data mining, and custom client requests
Participate in client meetings, as appropriate, to understand data collection and reporting requirements
Create and/or review functional and technical specifications based on user requirements
Partner with Data Management to support data review and issue resolution activities
Contribute to process improvements, SOP development, and documentation related to Clinical Data Programming
Assist with onboarding and training of team members, as needed

Bachelor’s degree in Life Sciences, Computer Science, or a related field preferred
SAS Base certification required
Experience developing programs using advanced SAS procedures; exposure to Python is beneficial
Understanding of database design, data structures, and clinical data workflows
Familiarity with the pharmaceutical drug development process
Experience working with CDISC SDTM standards and domains (e.g., EG, CO, DM, RE, VS, SUPP)
Strong analytical, problem-solving, and organizational skills
High attention to detail with a commitment to data quality
Effective written and verbal communication skills
Proficiency with Microsoft Office tools
Fluency in English (spoken and written)

Clinical Data Programmer I

Key skills