Clinical Data Scientist
1 day ago
Sponsor-dedicated:
You will be at the heart of our client's innovation, working fully embedded within one of our global pharmaceutical clients. This company is driving the next generation of patient treatment, empowering individuals with autonomy and ownership.
Position Overview:
This role involves leveraging advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead Phase I-IV clinical trials.
Responsibilities- Data manipulation, analysis, and reporting of clinical trial data using SAS programming
- Generating and validating SDTM and ADaM datasets/analysis files and tables, listings, and figures
- Production and QC/validation programming
- Generating complex ad-hoc reports using raw data
- Efficacy analysis
- Creating and reviewing submission documents and eCRTs
- Communicating with internal cross-functional teams and clients for project specifications, status, issues, or inquiries
- Lead duties when called upon
- Bachelor's degree in Statistics, Computer Science, Mathematics, etc.
- At least 7 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
- Experience implementing the latest CDISC SDTM/ADaM standards
- QC/validation skills
- Ad-hoc reporting skills
- Efficacy analysis proficiency
- Familiarity with drug development life cycle and experience manipulating, analyzing, and reporting clinical trials' data
- Submissions experience utilizing define.xml and other submission documents
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