Clinical Data Management Specialist
2 weeks ago
Job Opportunity
We are seeking a skilled SAS Developer to collaborate with our global Data Management team.
Please note that the official PSI CRO job title will be: Database Developer.
This role is ideal for individuals who are passionate about providing comprehensive clinical database development and programming services, ensuring high-quality, accurate, and consistent clinical data, and being part of a dynamic and challenging environment.
Responsibilities:
- Act as a liaison between data management and statistics teams on matters of database programming and deliverable database development
- Review and test clinical database (EDC) requirements/structure
- Review and program data validation plans and procedures
- Generate clinical database listings and reports to support clinical trial data collection, tracking, review, and validation
- Program patient profiles
- Contribute to the development of Study Data Tabulation Model (SDTM), annotated CRF, reviewer's guide, and program data transformation from raw data sources into CDISC-compliant deliverables
- Validate clinical trial data according to SDTM specifications
- Transfer deliverable databases to clients; facilitate electronic data transfers
- Liaise with vendors and clients regarding electronic data transfer specifications
- Receive and validate electronic data transfers
Requirements:
- College or University degree in IT, programming, or technical education
- 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 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
Additional Information
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