Senior Clinical Data Programmer
ClarioClario is expanding its Digital Physiology team in the UK and is hiring a Senior Clinical Data Programmer.
In this role, you’ll develop and test SAS code, review data specifications, and collaborate with Data Managers to ensure accurate data file creation. You’ll also support program validation, quality control, and ad-hoc programming, while driving process improvements and becoming a Subject Matter Expert (SME) in key offerings. Join us to help shape the future of healthcare through high-quality data solutions.
What we offer
Competitive compensation
Attractive benefits (security, flexibility, support and well-being)
Remote working with full technology setup
What you'll be doing
Develop and test SAS code for standard and custom data file creation
Review Clario’s data specifications and collaborate with Data Managers to finalize them
Attend client meetings to understand data collection needs
Validate encoding programs and perform ad-hoc programming for:
Quality control checks
Data resolution/mining
Client-specific requests
Gain exposure across modalities and become an SME in our top 5 offerings
Review user requirements and contribute to functional and technical specifications
Support Data Management with programming for data review
Participate in internal/external audits and represent Clinical Data Programming in NPI processes
Identify and implement process improvements
Contribute to best practices for quality, efficiency, and effectiveness
Act as CDP SME in cross-functional meetings
Mentor new team members and support onboarding
Help develop SOPs and related documentation
Complete administrative tasks as needed
What we look for
BS/BA in Life Sciences, Computer Science, or related field
SAS Advanced Certification
10+ years of SAS programming experience in pharma or CRO, including SAS/Base, SAS/Macro, SAS/SQL
1+ years in database design and data structures
5+ years in pharmaceutical or healthcare industry
Strong organizational, analytical, and communication skills
Detail-oriented with experience in CDISC SDTM and Define standards (e.g., EG, CO, DM, RE, VS, SUPP)
Proficiency in Windows and Microsoft Office
Fluent in English (spoken and written)
Experience with other programming languages is a plus
Proven ability to work with large, complex patient data sets
Knowledge of technical and regulatory requirements
Excellent time management across multiple projects
At Clario, 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.