DM/STDM Programmer

Salary: £49,000 - 89,000 per year

Requirements:

• We are looking for a technically minded person with strong communication skills and SDTM knowledge.
• We require experience in Study Design, CRF annotation, CDISC standards, vendor management, and SAS programming.
• We need at least 5 years of relevant experience in SDTM and/or CRF design.
• We require experience with biometrics processes, including review of SDTM annotated CRFs, writing and reviewing technical specifications, review of log files for errors and warnings, and resolving/troubleshooting errors.
• We require experience with data mapping and SDTM Controlled Terminology.
• We require experience with SAS programming and SDTM deliveries.
• We require prior experience in a clinical or pharmaceutical related field.
• We require prior experience in a data management related field.
• We require experience with relational databases, preferably Clinical Data Management and EDC systems.
• We require advanced familiarity with reporting tools.
• We require advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices.
• We require excellent verbal and written English.

Responsibilities:

• We work with the client directly to manage Database CRF and SDTM deliveries.
• We oversee all activities related to SDTM end to end.
• We manage CRF design from the protocol.
• We ensure vendor specifications are compliant with SDTM needs.
• We define SDTM specifications on some studies and/or provide SDTM review and oversight.
• We ensure quality and completeness of SDTM format data.
• We collaborate with sponsor colleagues and CRO partners to review CRF design and compliance with standard and SDTM.
• We work with Study Data Leads to plan for data receipt and oversee it throughout assigned clinical trials.
• We program reports and contribute to the standardization of processes and reports used for data review and analysis for external partners, vendors, and internal teams.
• We complete formal and ad-hoc analyses and oversee SDTM data.
• We review critical documents and deliverables, including SDTM annotation and SDTM datasets, to ensure data standards are used consistently and support creation of the DE dataset.
• We map SDTM data and manage annotated CRFs.
• We attend meetings as applicable with Mission, Submission, Project, Program, JCST, DEM, Biometrics, Clinical & Regulatory Solutions Team, and Early Phase.
• We perform relevant quality checks and create standard edit checks for new CRF modules.
• We support audits and inspections as required and take on other responsibilities and projects as assigned.

Technologies:

• Support
• SAS

More:

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. This role is part of a sponsor-dedicated project and can be based remotely from anywhere in Europe or in South Africa. Possible locations include the UK, Spain, Belgium, South Africa, Romania, Hungary, Ireland, France, Italy, Czech Republic, and Bulgaria. The summary location listed is Reading, Berkshire, United Kingdom, and the position is full time. We are committed to integrity in our hiring process and maintain a zero tolerance policy for candidate fraud.

last updated 36 week of 2026