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SMB Cert: 8(a), DGS, MBE Cert: NCMSDC, VMSDC, CPUC GSA Schedule 70
newark, CA, United States

Phone: 5108702224
Web Site: www.kutircorporation.com

Company Profile

Sr. Clinical Data Programmer/Analyst


Job ID:



Pleasanton, CA, United States 


Health-Care, Pharmaceutical


$50.00 per hour

Job Views:


Employment Type:

Contract - Corp-to-Corp, Contract to Hire - W2, Contract - W2, Contract - 1099



Job Description:

Position: Sr. Clinical Data Programmer/Analyst
Location: Pleasanton CA
Duration: 6+ months
Job Description/Responsibilities:
Department: Medical Affairs - Data Management
  • Develop scripts and programs to used to capture, manage, and analyze clinical data and study metadata.
  • Automate data management processes using multiple technologies:  Medrio EDC, independent programs, SAS programs or Microsoft Office macros.
  • Create custom data management listings by study, program, or other requests, as needed
  • Create custom reports to support data management metrics or ad-hoc study reports, as needed
  • Facilitate the data management report specification process and it’s requests; includes review, interpretation, and guidance on the report specifical requests prior to performing.
  • Database software development experience is requirement and application development and validation is a plus
  • Review database build programming specifications and Data Transfer Agreements.
  • Advises non-technical personnel on data retrieval and browsing of SAS generated reports.
  • Familiarity with querying/reporting tools, such as Tableau, Crystal, Office Analytics, etc.
  • Software and application development and validation (e.g., API), if needed
  • Support database development, as needed
  • Perform other technical duties as requested
  • B.S. degree in Computer Science or related field, or equivalent combination of education and work-related experience.
  • Extensive knowledge of SQL, Visual Basic (or VBA) and Windows script programming
  • At least 3 years working with clinical data management systems (Medrio EDC preferred)
  • At least 5 years of pharmaceutical, biotech, medical device and/or diagnostic industry experience
  • Experience in SAS / SQL programming
  • Knowledge of GCP and FDA requirements regarding clinical data management documentation and software.
  • SAS Programming
  • Project & Time Management
  • MS Excel- Advanced
  • MS Office/Powerpoint/Project office
  • Familiarity with EDC applications (e.g. Medrio, Inform, RAVE)
  • C+ Sharp a plus
  • Java (a plus)

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