
Senior Quantitative Analyst
11 hours ago
Sponsored by a leading pharmaceutical client, you will work as a Senior Statistical Programmer within a global team.
This role can be performed remotely and offers the opportunity to work on Phase I-IV clinical trials with advanced SAS programming skills and proficiency in CDISC standards.
Key Responsibilities:- Data manipulation, analysis, and reporting 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 teams and clients for project specifications, status, issues, or inquiries
- Bachelor's degree in Statistics, Computer Science, Mathematics, etc.
- At least 7 years of SAS programming experience with clinical trial data in the Pharmaceutical & Biotech industry
- Study lead experience, preferably juggling multiple projects simultaneously
- SAS data manipulation, analysis, and reporting skills
- CDISC SDTM / ADaM standards implementation
- QC/validation skills
- Ad-hoc reporting skills
- Efficacy analysis proficiency
- Drug development life cycle experience and clinical trials' data manipulation, analysis, and reporting
- Submissions experience using define.xml and other submission documents
- Opportunity to work with autonomy and ownership
- Collaborative cross-cultural environment
- Flexible remote work arrangement
We are looking for a highly skilled and experienced Senior Statistical Programmer to join our team. If you have a strong background in SAS programming and a passion for working on complex clinical trials, we encourage you to apply.
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