Bodhi Global Solutions
Sr. Clinical SAS Programmer
South San Francisco, CA
September 16, 2019
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.
6 to 10 (Yrs)
Required Skill Set
CDISC, ADaM, SDTM, tfl
$60 - $70/hr
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Sr Clinical SAS Programmer with strong CDISC experience
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