- Accountable for the quality and timely delivery of datasets and displays required for their clinical study
- Works with statisticians and programming leads to ensure clear specifications for their programmed deliverables are in place.
- 3 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.
- Statistical Programming and SAS hand-on experience
- Clinical trials expertise with an understanding of data operations required
- Working knowledge of clinical data and relevant data standards and at least 1 Therapeutic Area
- CDISC experience desirable
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