Sr. Clinical SAS Programmer

  • South San Francisco, CA
  • September 16, 2019
Responsibilities:
  • Over 6 years of experience as clinical SAS programmer 
  • Independently develop SAS and specifications (e.g. SDTM, ADaM), for use in study or other analyses, such Integrated Safety Summaries.
  • Independently develop datasets in SDTM and ADaM format and to clearly document the process that was followed in the form of specifications, Pinnacle 21 reports, trackers, and checklists.
  • Responsible for programming QC and oversight of CRO deliverables such as analysis datasets and tables, listings, and figures (TLFs).
  • Must be able to program defensively, check results, and consistently produce accurate output.
  • Independently verify other programmer’s results.
  • Adhere to FDA regulations regarding training records, guidelines, work instructions, and SOPs.
  • Produce study datasets and programs that will help meet CDISC standards and regulatory requirements.
  • Support Ad-hoc requests as needed such as outputs for manuscripts and conference abstracts and presentations.
  • Assist team to ensure timelines for the study and/or project are met.
  • Assist with training new employees or contractors, in particular on study specifics and departmental programming conventions and standards.

Experience

6 to 10 (Yrs)

Required Skill Set

CDISC ADaM SDTM Tfl

Salary

$60 - $70/hr

Telecommute

No

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Sr Clinical SAS Programmer with strong CDISC experience