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Title: Sr. Clinical Data Programmer

Company: i3 Statprobe (a UnitedHealth Group company)

Location: any i3 Statprobe office - Ann Arbor, MI, Austin, TX, Basking Ridge, NJ, Cary, NC, Eden Prairie, MN, Lexington, KY, San Diego, CA or Burlington, Ontario, Canada.

Salary: dependent upon experience

Job Description:

i3 Statprobe focuses exclusively on providing the pharmaceutical and biotechnology industries with comprehensive, integrated data service solutions that include data capture, summary, analysis and reporting for clinical trials across all phases of research.

The Sr. Clinical Data Programmer is responsible for all clinical programming on a study, including planning, construction, testing and maintenance of clinical databases in Oracle Clinical, SAS, or other DBMSs (i.e. ePower, DataFax).

Responsibilities

  • Oversees or completes planning, construction, testing and maintenance of clinical databases for assigned studies
  • Reviews database structures and programming in area of expertise (i.e. Oracle Clinical, SAS or other DBMSs)
  • Reviews Case Report Forms and Data Management Plans
  • Incorporates all external data sources (e.g. lab, ECG) in clinical database
  • Acts as programming contact with data management and sponsor team to address database issues and provide technical expertise as needed
  • May mentor or provide line management to clinical data programmers

Qualifications

  • BS degree and clinical data programming experience
  • Proficiency in Oracle Clinical, SAS or other DBMSs to set-up, program and administer clinical databases
  • Excellent people and communication skills (written and oral)
  • Experience working with lab and other third-party data
  • Demonstrated programming and logic skills

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For immediate consideration, please email your resume to Pam Livingston - pamela.livingston@i3global.com. You can also view all of our open positions by going to www.i3careers.com.



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