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.