Clinical Data Programmer I

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.