Lead SAS Programmer for Clinical Trials
4 days ago
Job Overview
We are seeking a highly skilled Lead SAS Programmer to join our team at Lifelancer. As a key member of our pharmaceutical clients' innovation team, you will leverage your advanced SAS programming skills and proficiency in CDISC standards to support or lead one or more Phase I-IV clinical trials.
Key Responsibilities
- Data manipulation, analysis, and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming
- Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs)
- Production and QC/validation programming
- Generating complex ad-hoc reports utilizing raw data
- Applying strong understanding/experience of Efficacy analysis
- Creating and reviewing submission documents and eCRTs
- Communicating with internal cross-functional teams and clients for project specifications, status, issues, or inquiries
Requirements
- Bachelor's degree in Statistics, Computer Science, Mathematics, etc.
- At least 8 years of SAS programming experience working with clinical trial data in the Pharmaceutical Biotech industry
- Study lead experience, preferably juggling multiple projects simultaneously
- Strong SAS data manipulation, analysis, and reporting skills
- Solid experience implementing the latest CDISC SDTM/ADaM standards
- Strong QC/validation skills
- Good ad-hoc reporting skills
- Proficiency in Efficacy analysis
- Familiarity with drug development life cycle and experience with manipulating, analyzing, and reporting clinical trials' data
Salary Range
$120,000 - $180,000 per year, depending on experience
About Us
Lifelancer is a talent-hiring platform connecting professionals with opportunities in Life Sciences, Pharma, and IT. We value scientific rigor, collaboration, and innovation in our work.
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