Our client is a growing pharmaceutical company focused on neurology,dedicated to developing products for unmet needs in the treatment of Central Nervous System disorders.
This person will participate in the day-to-day management of CRO Data Management activities (i.e., development Data Management Plan (DMP), develop and annotate CRF's, develop database specifications, design or oversee the development of edit check specifications and programs, adherence to timelines and data expectations, etc.
POSITION SUMMARY: To provide SAS programming support for the Clinical Research Programming Department. ESSENTIAL FUNCTIONS:1. Develop and document programs to create analysis datasets summarizing key clinical trial data. 2. Develop and document programs and to produce tables, listings and other reports and analyses summarizing clinical trial results.
Leading Pharmaceutical fortune 200 company with over 25,000 employees globally is seeking to expand its team in the Bay Area. While the company is international, this team has more of a small company feel, looking for the right cultural fit for this Sr.
East Bay client in need of a process validation engineer with commercial scale chromatography experience.9 month initial contract with possibility of extension.
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