Company:
Katalyst Healthcares & Life Sciences
Location: South Plainfield
Closing Date: 20/10/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
Responsibilities:
Creates standard and/or custom programs/reports using data analytics tools such as SAS, or other data visualization tools to support data oversight and review by data managers or other data reviewers.
Collaborates with cross-functional groups to develop standard and custom data reports for quality data oversight / clinical data review.
Assists in the management of electronic data from external data sources/vendors in partnership with the DM team.
Liaises with vendors as needed to facilitate electronic data transfers and/or data specification requirements.
Assists in review and approval of required study documentation, including design specifications, user requirements, data transfer specifications and data standards.
Other related responsibilities as required.
Requirements:
8-10 years of programming experience in the Biotech/Pharmaceutical industry working for a sponsor company.
Ability to work independently to create standard datasets, program edit checks and produce quality data review outputs.
Demonstrated understanding of CDISC and SDTM & ADaM requirements and implementation guidelines, able to create and validate CDISC standard datasets.
Experience creating source and validation programs using SAS software for analysis datasets, and tables, listings, and graphs (TLGs) for multiple studies/products.
Creates standard and/or custom programs/reports using data analytics tools such as SAS, or other data visualization tools to support data oversight and review by data managers or other data reviewers.
Collaborates with cross-functional groups to develop standard and custom data reports for quality data oversight / clinical data review.
Assists in the management of electronic data from external data sources/vendors in partnership with the DM team.
Liaises with vendors as needed to facilitate electronic data transfers and/or data specification requirements.
Assists in review and approval of required study documentation, including design specifications, user requirements, data transfer specifications and data standards.
Other related responsibilities as required.
Requirements:
8-10 years of programming experience in the Biotech/Pharmaceutical industry working for a sponsor company.
Ability to work independently to create standard datasets, program edit checks and produce quality data review outputs.
Demonstrated understanding of CDISC and SDTM & ADaM requirements and implementation guidelines, able to create and validate CDISC standard datasets.
Experience creating source and validation programs using SAS software for analysis datasets, and tables, listings, and graphs (TLGs) for multiple studies/products.
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