Need SAS Clinical Programmer *Menlo Park, CA* *Long Term* *Please send your resumes to [email protected]*
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 -- You received this message because you are subscribed to the Google Groups "Android Developers" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To view this discussion on the web visit https://groups.google.com/d/msgid/android-developers/ffa78f97-cd50-4540-b386-c141b4ac2657%40googlegroups.com.
