Developer, Clinical Data Applications & EDC Systems

Main Responsibilities And Accountabilities

• Drive activities related to the design, development, and maintenance of clinical study databases by applying advanced technical expertise in: CRF design; database build; edit check programming; report development; custom programming; system interface configuration; and the implementation of all relevant systems features to support high-quality, compliant clinical data management.
• Collaborate with clinical study teams, Standards (CDASH/SDTM,CSL), and cross-functional stakeholders to define, implement, and continuously enhance data quality methods, acceptance criteria, and validation rules for eCRF and external data sources across all study models.
• Oversee the implementation and maintenance of data quality control frameworks, including validation check libraries and acceptance criteria for vendor and internally generated data, ensuring alignment with CSL standards and regulatory expectations.
• Govern and maintain a standardized library of reports and listings to support study teams, ensuring consistency, reusability, and efficiency across in-house, hybrid, and vendor-supported studies.
• Oversee the setup, automation, and monitoring of recurring data quality and operational reports across different models (in-house vs outsourced etc.), ensuring accuracy, completeness, and timely availability of outputs.
• Partner with Data Management, Statistics, and vendors to review and validate clinical data deliverables, ensuring submission readiness in accordance with regulatory standards (e.g., SDTM, define.xml).
• Lead the reporting solutions that provide insights into data quality, study progress, and key metrics to support informed decision-making.
• Ensure appropriate data structures, storage, and integration approaches that enable pooled analyses, traceability, and efficient retrieval of both current and legacy clinical data.
• Support the integration and governance of external data sources (e.g., IxRS, eDiaries, labs, ECG), ensuring data consistency, quality, and alignment with study requirements, while facilitating collaboration between internal teams and vendors.
• Contribute to innovation and future-state initiatives by supporting the development of scalable data platforms, automation strategies, and AI-enabled capabilities to enhance data processing, validation, and analytics.

Job Qualifications And Experience Requirements

• 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.
• Exposure to in-house, hybrid, and/or vendor-supported study models.
• 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, data quality oversight, validation processes, and vendor deliverable review.
• Proven ability to manage priorities, meet timelines, and operate effectively in a fast-paced and evolving environment.
• Experience with C# is preferred and familiarity with SAS, Python, or R is a plus.