About this role
At Clario, a part of Thermo Fisher Scientific, we are transforming clinical trials through innovative data solutions that improve patient outcomes. As a Clinical Data Programmer I, you will support the development, validation, and delivery of clinical datasets, working closely with cross-functional teams to ensure high-quality, compliant data outputs across studies.
What We Offer
• Competitive compensation and benefits package
• Flexible remote working environment
• Opportunities for career growth and exposure to multiple clinical modalities
• A collaborative, global team focused on advancing clinical research
What You’ll Be Doing
• 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
What We Look For
• 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)
At Clario, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.