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Data Standards Manager
Job in
South Plainfield, Middlesex County, New Jersey, 07080, USA
Listed on 2026-09-21
Listing for:
Katalyst CRO
Full Time
position Listed on 2026-09-21
Job specializations:
-
IT/Tech
Information Security & Data Protection, Information & Knowledge Management, Data Analyst, Data Warehousing
Job Description & How to Apply Below
- eCRF Design
- Able to critically review eCRF designs to ensure compatibility/conformance with CDASH/SDTM standards. - Recognizes limitations in eCRF design and works with the study team to correct flaws proactively.
- SDTM Conformance Mapping Create and Reviews SDTM conformance mapping specifications applying SDTM, TAUG and Client standard.
- CDISC Validation Tools
- Executes validation tools (e.g., Pinnacle 21) and collaborates with other functions to resolve identified issues. - Ensure any unresolved issues are appropriately documented (e.g., Clinical Study Data
- Create and review Trail Design domains
- Clear understanding of End-to-end traceability from Data Collection to Data reporting. Metadata Repository
- Responsible for managing libraries of CDISC-related metadata, terminology, and related standards within the metadata repository. - Provides governance oversight to Data Standards Analyst and Sr Data Standards Analyst to ensure consistency in metadata.
- Standards Development Assist in the development of data standards.
- Standards Governance Provide guidance to study team members on the appropriate use of Client's standards. Consult on complex study-specific data collection and mapping to SDTM.
- Cross-functional Team Participation Represents the Clinical Data Reporting & Standards group to ensure industry and Client standards are followed and understood.
- Communication
- Clearly communicates an understanding of clinical data standards concepts, clinical principles, and regulatory guidance and acts in accordance with those principles. - Effectively presents data standards concepts and logical arguments to statistical programmers, statisticians, data scientists, clinical development and regulatory study team members.
- Able to diplomatically and persuasively represent the interests of the Data Standards group in cross-functional initiatives.
- eCRF Design
- Able to critically review eCRF designs to ensure compatibility/conformance with CDASH/SDTM standards. - Recognizes limitations in eCRF design and works with the study team to correct flaws proactively.
- SDTM Conformance Mapping Create and Reviews SDTM conformance mapping specifications applying SDTM, TAUG and Client standard.
- CDISC Validation Tools
- Executes validation tools (e.g., Pinnacle 21) and collaborates with other functions to resolve identified issues. - Ensure any unresolved issues are appropriately documented (e.g., Clinical Study Data
- Create and review Trail Design domains
- Clear understanding of End-to-end traceability from Data Collection to Data reporting. Metadata Repository
- Responsible for managing libraries of CDISC-related metadata, terminology, and related standards within the metadata repository. - Provides governance oversight to Data Standards Analyst and Sr Data Standards Analyst to ensure consistency in metadata.
- Standards Development Assist in the development of data standards.
- Standards Governance Provide guidance to study team members on the appropriate use of Client's standards. Consult on complex study-specific data collection and mapping to SDTM.
- Cross-functional Team Participation Represents the Clinical Data Reporting & Standards group to ensure industry and Client standards are followed and understood.
- Communication
- Clearly communicates an understanding of clinical data standards concepts, clinical principles, and regulatory guidance and acts in accordance with those principles. - Effectively presents data standards concepts and logical arguments to statistical programmers, statisticians, data scientists, clinical development and regulatory study team members.
- Able to diplomatically and persuasively represent the interests of the Data Standards group in cross-functional initiatives.
- MS with 8 years of relevant clinical research experience (or BS with 12 years relevant experience).
- Expert level of knowledge of CDASH, SDTM, define.xml and controlled terminology. Experience in mapping and converting legacy data into SDTM domains for eCTD submissions.
- Minimum of two successful submissions of CDISC compliant data.
- Knowledge of international regulations, requirements and guidance associated with clinical data standards and the preparation of data sets for regulatory submission.
- Experience with metadata repository technology and its application in clinical data standards processes and experience with data standards governance.
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