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Clinical SAS Programmer
Location: US-CA-Menlo Park
Jobcode: 1a9282ed368fe87c6d26abea69dd556d-122020
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SAS Clinical Programmer
Menlo Park, CA
Long Term
Client is committed to helping patients defeat their cancer. they are advancing immune-oncology through the engagement of new and complementary phagocytic pathways that enhance anti-tumor efficacy and selectivity.
Summary: The Clinical Programmer is responsible for developing program specifications, programming listings and reports, and providing other clinical programming support for assigned studies.
Essential Functions:
These may include, but are not limited to, the following; other duties may be assigned
• Develop SAS programs for data cleaning, reconciliation, review and status updates
• Execute and/or distribute data management metrics, listings, and reports, as required
• Review and contribute to the development of data transfer specifications
• Responsible for clinical data downloads and data transfers to/from service providers
• Create reports in Medidata RAVE using J-Review or Business Objects
• Manage clinical programming and EDC system timelines to coordinate and synchronize deliverables with the overall study timelines
• Responsible for execution of ad hoc programming requests, and other reports as required
• Participate in CRF design, EDC setup and testing to ensure consistent data standards
• Contributes to decisions regarding the technical infrastructure of data management and works with IT to ensure local IT infrastructure meets clinical data management needs and global standards
• Develop and implement strategy for the improvement of productivity and standardizing of study build, database setup and programming activities
• Follow good programming practices and documentation
Education & Experience:
• Bachelor degree in Life Sciences, Computer Sciences, or Mathematics with a minimum of 5 years of data management and SAS programming experience in the pharmaceutical or biotechnology industry
• Prior oncology/hematology experience highly desirable
• Requires solid knowledge of clinical data management principles, clinical trials process and regulatory requirements
• Competent in SAS programming, including macros
• Strong well-rounded technical skills (SAS, EDC systems, MS Word, Excel, PowerPoint) and knowledge of industry standards (CDISC, SDTM, CDASH)
• Excellent verbal/written and interpersonal skills required for working successfully in a cross-functional team environment
• Good working knowledge of ICH, FDA, and GCP regulations and guidelines;
• Experience with Business Objects, J-Review, Rave Web Services, and other Medidata modules and reporting tools strongly preferred
Omega solutions inc (Confidential Company)
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