PSI CRO
Contract Research Organization
SeniorDatabaseDeveloper
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“Senior Database Developer at PSI CRO. Skills: SAS programming, SDTM, CDISC standards. Communicate database programming matters. Develop deliverables database”
Industry & Context.
What They're Looking For.
Must Have
Full working proficiency in English, Sufficient relevant technical experience
Nice to Have
Experience in Clinical Data Management systems, Experience in a professional environment, preferably with clinical or medical data
What You'll Do.
Communicate database programming matters
Develop deliverables database
Review clinical database requirements
Test clinical database structure
Review data validation plan
Program data validation procedures
Generate clinical database listings
Generate reports for data collection
Program patient profiles
Support SDTM development
Program data transformation
Validate clinical trial data
Transfer deliverable database
Receive electronic data transfers
Validate electronic data transfers
How You'll Work.
Team & Collaboration
Data management teams; Statistics teams
Full Job Description
PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. 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! Responsibilities: * 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 ## Qualifications * 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 l
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