Senior SAS Developer, SDTM

🕒 June 10

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PSI CRO AG

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1996

⚕️ Healthcare Insurance

💊 Pharmaceuticals

🔬 Science

Healthcare Insurance • Pharmaceuticals • Science

PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.

📋 Description

• 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

🎯 Requirements

• 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.

🏖️ Benefits

• Excellent and flexible working conditions • Extensive training • Friendly, collegial team • Competitive salary and benefits package • Opportunities for personal and professional growth