
Senior Data Analyst
2 days ago
We are seeking a highly skilled Senior Statistical Programmer to drive innovation and empower individuals to work with autonomy and ownership. This role offers flexibility, allowing for remote work.
This is a sponsor-dedicated opportunity where you will be embedded within one of our pharmaceutical clients, leading or supporting Phase I-IV clinical trials by leveraging advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM).
Key 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.
- Complex ad-hoc reports using raw data.
- Efficacy analysis.
- Creating and reviewing submission documents and eCRTs.
- Communication with internal cross-functional teams and clients for project specifications, status, issues, or inquiries.
To be successful in this role, you will need:
- Bachelor's degree in Statistics, Computer Science, Mathematics, or related field.
- 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.
- 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 clinical trials' data manipulation, analysis, and reporting.
This role offers flexibility, allowing for remote work, and the opportunity to work on complex and innovative projects.
OthersIf you are a motivated and detail-oriented individual with excellent analytical and troubleshooting skills, we encourage you to apply for this exciting opportunity.
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