PSI CRO

Contract Research Organization

SeniorDatabaseDeveloper

€45–65k ~AI est. Zagreb, Croatia FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for not-applicable candidates.

The Brief

“Senior Database Developer at PSI CRO. Skills: SAS Development, SDTM, CDISC Standards. Serve as communication point for database programming. Deliver database development”

Industry & Context.

Contract Research Organization

What They're Looking For.

Must Have

Full working proficiency in English, Sufficient relevant technical experience, Knowledge of and experience in the SAS programming language, Knowledge of CDISC standards, Knowledge of and experience in SQL, Proficient user of standard MS Office applications

Nice to Have

Experience in Clinical Data Management systems, Experience with MS Access

What You'll Do.

Serve as communication point for database programming

Deliver database development

Review clinical database requirements

Review clinical database structure

Test clinical database structure

Review data validation plan

Program data validation procedures

Generate clinical database listings

Generate clinical database reports

Program patient profiles

Support SDTM development

Program data transformation

Validate clinical trial data

Transfer deliverable databases

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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