
Senior Data Analyst
2 days ago
Job Overview:
We are seeking a skilled Statistical Programmer to join our team. In this role, you will be responsible for data manipulation, analysis and reporting of clinical trial data.
- Performing 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
Key Responsibilities:
- Support or lead one or more Phase I-IV clinical trials
- Collaborate with cross-functional teams to deliver project specifications, status, issues or inquiries
- Communicate effectively with internal and external stakeholders
- Perform 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
- Strong SAS data manipulation, analysis and reporting skills
- Solid experience implementing the latest CDISC SDTM / ADaM standards
- Good ad-hoc reporting skills
- Opportunity to work on exciting projects with global pharmaceutical clients
- Chance to collaborate with talented professionals from diverse backgrounds
- Professional growth and development opportunities
- Experience supporting immunology, respiratory or oncology studies is a plus
- Excellent analytical & troubleshooting skills
- Ability to work effectively and successfully in a globally dispersed team environment
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