DM/STDM Programmer
IQVIA · Berkshire, UK
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Role summary
IQVIA seeks a DM/STDM Programmer to oversee database and data standardization deliverables for a sponsor-dedicated clinical trial project. The role manages CRF design, SDTM compliance, vendor specifications, and data quality across studies, requiring five years' experience in SDTM/CRF design, SAS programming, biometrics processes, and clinical data management. Remote work available across Europe and South Africa.
What they're looking for
- At least 5 years experience in SDTM and/or CRF design
- SAS programming skills with SDTM deliveries
- Experience reviewing SDTM annotated CRFs and writing technical specifications
- Knowledge of data mapping, SDTM controlled terminology, and relational databases
- Clinical or pharmaceutical field background with data management experience required
- Advanced familiarity with reporting tools and federal regulations, GCP, GCDMP
- Fluent English communication skills, verbal and written
What you'll be doing
- Oversee all end-to-end SDTM activities and manage CRF and SDTM deliveries with sponsor clients
- Collaborate with sponsor colleagues and CRO partners to review CRF design compliance with SDTM standards
- Program reports and quality checks for data review; manage annotated CRF and SDTM data mapping
- Review critical deliverables including SDTM annotations and datasets for data standards consistency
- Support audits, inspections, and attend cross-functional meetings as applicable
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.