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Standard job listing
Title of job: SAS PRINCIPAL PROGRAMMER
Job Location: Goleta, California, 93117
Job Type: Contract to Hire
Price Range:
Negotiable, Depending on experience
Start Date:
ASAP
End Date:
Not a pressing concern
Categories:
# Section Category Subcategory
#1 Technical Information Systems Database Developer
Qualifications:


Other desired skills:
SAS PRINCIPAL PROGRAMMER
Job/Project Details: SAS Programmer IMPORTANT! ALL APPLICANTS MUST MEET ALL JOB REQUIREMENTS TO APPLY. JOB SUMMARY: Under general guidance, will create, test, validate, implement and maintain clinical studies in Oracle Clinical (OC). Instrumental in the creation of SQL, PL/SQL and SAS programs used for review, clean-up and transfer of data collected during Clinical Trials. Oversee as well as develop, test, validate and implement edit check/validation procedures in OC used for review of data collected during Clinical Trials REQUIREMENTS: o Bachelor's or Masters in Computer Science or other relevant degrees with 5+ years of pharmaceutical experience preferred o The work experience should include at least two years of technical leadership in a clinical programming environment in a pharmaceutical or biotechnology setting and a knowledge of clinical trial methodology, GCP, and FDA regulations and guidelines, including 21 CFR Part 11 is preferred. o Working knowledge and experience with OC application and the Oracle relational database system o Programming knowledge of SQL and PL/SQL and knowledge of the UNIX operating systems and familiar with vi o Experience and knowledge of SAS programming as well as experience with iREVIEW report creation would be an added asset o Excellent analytical, problem solving, and computer skills. o Flexible, well organized, excellent verbal and written communication and interpersonal skills. o Able to give effective presentations to small groups such as Implementation Teams or Clinical meetings o Works well under pressure, with initiative to take on unfamiliar tasks o Encourages mutual respect and accountability at all levels KEY DUTIES AND RESPONSIBILITIES: o This position has no direct supervisory responsibility, however will provide direction and leadership to employees assigned to project teams and provide input on their performance o Responsible for the creation/maintenance of all new and existing studies in OC. o Take a lead role in OC programming to generate listings per adhoc requests and create/test validation procedures and any other requests pertaining to study builds for new and legacy studies. o Assist in the maintenance of legacy studies and in the resolution of the various queries related to them o Assist in the Development and implementation of new processes ensuring that Data Management programming policies, guidelines and procedures are followed during day-to-day assignments. o Take a lead role in the development, implementation and maintenance of standards in GLIB. Build up the GLIB as new studies are being created in OC. o Assist in the creation/maintenance of Standard Operation Procedures and Work instruction Manuals o Mentor the other study designers in the group.df-jb

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