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The ideal candidate will come from a pharmaceutical or Clinical Research organization having gained 1 year plus experience in a professional atmosphere. Advanced degree (MS or PhD) in statistics, or related field preferred BS qualifications (or equivalent) are required. In addition to an academic qualification, the statistical programmer will need to have at least one year experience working as a SAS statistical programmer within either a Pharmaceutical company or a CRO. The selected candidate will support the lead statistician on other projects; provide programming and QC support in the production of statistical appendices. Candidate needs to be a self-starter and have the ability to meet defined objectives with minimum supervision, a go-getter attitude to overcome all obstacles along the way. Persistence, focus, attention to details, commitment to excellence are critical for this position. We accept applications from exceptional candidates with less than 3 years but more than 1 year of clinical trial SAS programming experience.
Summary
• A motivated self starter with at least 1 year of industry and/or CRO experience working in clinical trials
• Excellent working knowledge of SAS and statistical analysis, proficient in SAS, SAS STAT and macro language
• Confident when dealing with internal and external customers, excellent verbal and written communication skills
• Assist in design of studies from a statistical point of view
• Strong knowledge of statistical principles underlying clinical trials and strong statistical skills
• Experience in medical device trials would be an asset
This is a position that offers substantial growth opportunities and excellent benefits for the right candidate that will work with the top pharma/biotech companies of the San Francisco Bay Area. Local candidates preferred.
Please send by email your resume for consideration. Principals only, we are not welcoming calls from recruiters.
- Compensation: Market
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