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# Senior SAS Developer (SDTM)

- **Company:** PSI CRO
- **Location:** Oxford, UK (Remote available)
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Microsoft Access, Clinical Data Management, Clinical Data Repository, Computer Programming, Databases, Data Validation, Data Transmissions, Data Transformation, Database Development, Microsoft Office, Standard Sql, SAS (Software), Extensible Markup Language (XML), Macros, Data Management, Veeva
- **Published:** June 11, 2026
- **Apply:** https://uk.indeed.com/viewjob?jk=4397afaa8fd2aecc

## About the Role

Do you have experience in XML?, Do you have a Bachelor's degree?, * College or University degree (IT, programming, technical education)

 * Full working proficiency in English
 * Sufficient relevant technical experience
 * Experience in Clinical Data Management systems (like Medidata/Veeva) is desirable
 * Knowledge of and experience in the SAS programming language (Base SAS, SAS/Macros, SAS/ODS)
 * Knowledge of CDISC standards
 * Knowledge of and experience in SQL
 * Proficient user of standard MS Office applications and MS Access
 * Experience in a professional environment, preferably with clinical or medical data

Only CVs in English will be considered.

## Description

We are currently looking for a knowledgeable and proactive SAS Developer to join our global Data Management team.
Please note the official PSI CRO job title will be: Senior Database Developer.

If you are keen to provide the full range of clinical database development and programming services, ensure high quality, accuracy, and consistency of clinical data, and be involved in something new, outstanding and challenging, this job opportunity is perfect for you!, * Communication point for data management and statistics on matters of database programming and deliverable database development

 * Clinical database (EDC) requirements/structure review and testing
 * Data validation plan review and programming of data validation procedures
 * Generation of clinical database listings and reports to support clinical trial data collection, tracking, review and validation
 * Programming of patient profiles
 * Participate and support the development of Study Data Tabulation Model (SDTM) (define.xml, annotated CRF, reviewer's guide) and programming of data transformation from raw data sources into CDISC-complaint deliverable
 * Validation of clinical trial data according to SDTM specifications
 * Deliverable database transfer to clients; electronic data transfers
 * Liaison with vendors and clients regarding electronic data transfer specifications
 * Receipt and validation of electronic data transfers


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