Posted:2 months ago|
Platform:
Work from Office
Full Time
QUALIFICATIONS / SKILLSBachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field. At least 4 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 for the reporting of clinical trial data. CDISC experience desirable JOB SUMMARY Summarize the primary purpose & key accountabilities of the job. A productive, hands on programmer who applies technical knowledge and practical experience to deliver statistical programming deliverables to support assets and study teams with limited supervision early in role and independently later in role Ensures excellence in the programming of analysis ready datasets, tables, listings, and figures for which they are responsible Ensures adherence to high quality programming standards in their daily work JOB RESPONSIBILITIES Indicate the primary responsibilities critical to the job. Accountable for the quality and timely delivery of datasets and displays required for their clinical study.
AVE-Promagne Business Solutions
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