Mgr, Database Management Systems

Experteer Overview In this role you will lead global database management and clinical data standards to support multicenter trials. You will serve as a subject matter expert in clinical data standards, Medidata Rave library development, and SAS programming, partnering with cross-functional teams to ensure high-quality, standardized data collection and reporting. You’ll drive governance and process improvements while mentoring junior staff, contributing to the company’s mission of accelerating the development of medicines. This is a hands-on, impact-driven leadership position with a clear focus on data quality, standards compliance, and scalable data solutions. Compensation / Benefits * Lead development and maintenance of global clinical data standards, including CDISC-compliant mappings and SDTM * Develop and maintain Medidata Rave global library objects (eCRFs, edit checks, CRF Completion Guidelines) * Create SAS programs for edit checks, data imports, listings, custom reports, and data validation * Construct clinical datasets from raw data using Base SAS, Advanced SAS, Macros, PROC SQL, and SAS ODS * Support CRF design, annotated CRFs, data mapping specs, and define.xml requirements * Collaborate with Clinical Data Management, Clinical Operations, EDC Programming, vendors, and CROs to ensure consistent standards * Drive process improvements, support governance committees, and mentor junior team members * Ensure compliance with CDISC standards, GCP, ICH, and regulatory requirements Tasks * Strong clinical domain knowledge across clinical trial phases * Experience in clinical research/pharma/biotech/healthcare/CRO * Hands-on SAS Edit Check Listings programming * SAS data import programming experience * Experience using SAS ODS for generating reports (RTF, PDF, HTML) * Experience reading raw data, creating data structures, handling missing values, troubleshooting * Ability to append/concatenate SAS datasets * Proficiency with PROC PRINT, PROC FREQ, PROC MEANS, PROC TRANSPOSE, PROC SQL * Strong SAS Macros and SQL programming experience * Experience creating SAS datasets from raw clinical data (status and efficacy) * Ability to develop project-specific macros/formats, load client data from external platforms, prepare datasets for delivery * Experience creating clinical listings and custom reports per business needs * Knowledge of Vendor Import Programming * Strong expertise in Base SAS, Advanced SAS, SAS Macros, SAS SQL, and SAS Grid * Excellent written and verbal communication skills Key requirements *

CRF validation * Construct clinical datasets from raw data using Base SAS, Advanced SAS, Macros, PROC SQL, and SAS ODS * Support CRF design, annotated CRFs, data mapping specs, and define.xml requirements * Collaborate with Clinical Data Management, Clinical Operations, EDC Programming, vendors, and CROs to ensure consistent standards * Drive process improvements, support governance committees, and mentor junior team members * Ensure compliance with CDISC standards, GCP, ICH, and regulatory requirements Tasks * Strong clinical domain knowledge across clinical trial phases * Experience in clinical research/pharma/biotech/healthcare/CRO * Hands-on SAS Edit Check Listings programming * SAS data import programming experience * Experience using SAS ODS for generating reports (RTF, PDF, HTML) * Experience reading raw data, creating data structures, handling missing values, troubleshooting * Ability to append/concatenate SAS datasets * Proficiency with PROC PRINT, PROC FREQ, PROC MEANS, PROC a aaaaaaaB_ PROC SQL * Strong SAS Macros and SQL programming experience * Experience creating SAS datasets from raw clinical data (status and efficacy) * Ability to develop project-specific macros/formats, load client data from external platforms, prepare datasets for delivery * Experience creating clinical listings and custom reports per business needs * Knowledge of Vendor Import Programming * Strong expertise in Base SAS, Advanced SAS, SAS Macros, SAS SQL, and SAS Grid * Excellent written and verbal communication skills Key requirements *