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 modalitiesA 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 preferredSAS 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.

Summary

Location:

United Kingdom Remote Type:
Full time