DM Programmer
IQVIA · Reading, UK
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
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
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