
Data Analysis Expert
6 days ago
Sponsor-dedicated, this position offers the opportunity to be at the heart of a global pharmaceutical client's innovation. The role involves working fully embedded within one of our clients, with the support of our team behind you.
Job Overview:
This is an exciting time to be part of our client's new program. As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials.
Your 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.
- Efficacy analysis.
- Creating and reviewing submission documents and eCRTs.
- Communicating with internal cross-functional teams and client for project specifications, status, issues or inquiries.
- Lead duties when called upon.
- Team player with willingness to go the extra distance to get results, meet deadlines, etc.
Requirements:
- 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 with a bachelor's degree or equivalent.
- Study lead experience, preferably juggling multiple projects simultaneously preferred.
- Solid experience implementing the latest CDISC SDTM / ADaM standards.
- Strong analytical & troubleshooting skills.
- Ability to provide quality output and deliverables, in adherence with challenging timelines.
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