Developer, Clinical Data Applications – EDC Systems

CSL

Developer specializing in clinical data applications at CSL Behring, focusing on design, oversight, and validation of clinical data management processes.

Posted 7/29/2026full-timeKing of Prussia • Massachusetts, Pennsylvania • 🇺🇸 United StatesMid-LevelSenior💰 $143,000 - $169,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical database design and data quality management, with a strong focus on EDC systems and CDISC standards. Proven ability to collaborate with cross-functional teams and oversee data integration and reporting solutions.

Highest-signal resume keywords

Clinical Database DesignEDC Systems ProficiencyCDISC Standards FamiliarityData Quality Control FrameworksMedidata Rave Study Builder Certification

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Data ProcessesData MappingData ValidationData MigrationECRF DesignC# ProgrammingSAS FamiliarityPython FamiliarityR Familiarity

Soft Skills

Priority ManagementTimely ExecutionAdaptability

Tools & Technologies

Medidata RaveVeeva Vault

Certifications & Qualifications

Medidata Rave Study Builder Certification

Industry Keywords

PharmaceuticalCRO EnvironmentCDASHSDTMData Quality Methods

Tech Stack

Tools & technologies

PythonVault

About the role

Key responsibilities & impact

Drive activities related to the design, development, and maintenance of clinical study databases
Collaborate with clinical study teams, Standards (CDASH/SDTM,CSL), and cross-functional stakeholders to define, implement, and continuously enhance data quality methods
Oversee the implementation and maintenance of data quality control frameworks
Govern and maintain a standardized library of reports and listings to support study teams
Oversee the setup, automation, and monitoring of recurring data quality and operational reports
Partner with Data Management, Statistics, and vendors to review and validate clinical data deliverables
Lead the reporting solutions that provide insights into data quality, study progress, and key metrics
Ensure appropriate data structures, storage, and integration approaches that enable pooled analyses
Support the integration and governance of external data sources
Contribute to innovation and future-state initiatives by supporting the development of scalable data platforms

Requirements

What you’ll need

BSc in Computer Science, Mathematics, Statistics or related area with relevant experience
Medidata Rave Study Builder Certification is preferred
5+ years of relevant experience with clinical database design in EDC systems within a pharmaceutical or CRO environment
Familiarity/practical experience with CDISC standards, particularly CDASH, SDTM including data mapping, validation, and activities supporting submission readiness
Proficiency with EDC systems (e.g., Medidata Rave, Veeva Vault) and understanding of eCRF design and clinical data collection frameworks
Strong understanding of clinical data processes, including data standards, data flows, and integration of eCRF and external data sources
Proven ability to manage priorities, meet timelines, and operate effectively in a fast-paced and evolving environment
Ability to independently perform data migration activities for post-production study changes is preferred
Experience with C# is preferred and familiarity with SAS, Python, or R is a plus

Benefits

Comp & perks

Health insurance
401(k) matching
Flexible working hours
Paid time off
Remote work options