Job title: Sr. Clinical programmer
Company: Katalyst Healthcares & Life Sciences
Job 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.
Expected salary:
Location: South Plainfield, NJ
Job date: Thu, 12 Sep 2024 23:38:52 GMT
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