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 SAS Programmer- Pharmaceutical Clinical Research

Details
Country: USA
Location: San Francisco CA
Total applied: 40
Location:US-CA-San Francisco

Base Pay:N/A

Other Pay:
compensation based on education and experienceEmployee Type:Full-Time Employee

Industry:Biotechnology Pharmaceutical

Manages Others:no
SAS Programmer- Pharmaceutical Clinical Research

Biopharmaceutical Company in San Francisco, CA is looking for a SAS Programmer to join their team!

Responsibilities (include, but are not limited to:)
-Review and understand study protocols and other clinical related materials.
-Actively participate in clinical sub-teams and chair Data Mgt. concerns with regards to programming parameters.
-Design and implement automated standardized Data Mgt. reports.
-Participate and coordinate with programming the development, testing, and de-bugging of clinical databases
-Create and provide support for standardized and ad-hoc SQL queries.
-Create and assist in the development of standardized validation specifications along standardized data definitions for implementation and support of CDISC.
-Maintain an overall knowledge of regulatory guidelines, industry standards, and new technologies.
-Communicate project status and key project issues to data management team lead and department management manger.
-Communicate back to the clinical team of post-mortem investigation on previous study design for continuous improvement
REQUIREMENTS
Bachelor's degree from a US Institution in Computer Science or related area (e.g. Math, Statistics)
At least 4 years of related Pharmaceutical or CRO experience
Min. 2 years experience with clinical systems such as CTMS, EDC, IVRS, Oracle Clinical, and/or other related technology.
Proficiency in Microsoft Access, SAS/Base, SAS/Macro, SAS/AF, SAS/EIS in a UNIX or Windows environment.
Experience with data integration and system dependencies.
Ability to develop, debug, maintain, and validate-project specific SAS programs to generate SAS datasets, summary tables, data listings, and graphic displays according to departmental standards.
Ability to work independently, strong attention to detail in composing materials, establishing priorities, scheduling and meeting deadlines.
Oncology therapeutic experience desirable


SAS, SAS, SAS programmer, MedFocus, Pharmaceutical, CRO, Biotech, tables, listings, clinical research
SAS, SAS, SAS programmer, MedFocus, Pharmaceutical, CRO, Biotech, tables, listings, clinical research
SAS, SAS, SAS programmer, MedFocus, Pharmaceutical, CRO, Biotech, tables, listings, clinical research
SAS, SAS, SAS programmer, MedFocus, Pharmaceutical, CRO, Biotech, tables, listings, clinical research
SAS, SAS, SAS programmer, MedFocus, Pharmaceutical, CRO, Biotech, tables, listings, clinical research

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