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Contract Position Contract Position Must have Clinical Trials Experience
Write New Drug Application submissions and Chemistry Manufacturing & Controls materials. Plan and prepare a variety of clinical documents (clinical study reports, investigator brochures, etc.) by organizing, analyzing, and interpreting scientific and statistical data. Prepare integrated summary documents for regulatory submissions. Participate in study teams, coordinate and conduct document-related meetings including the preparation of a pre-meeting agenda and post-meeting minutes. Review protocols, clinical data reports, and case report forms as required. Eight
Must have Clinical Trials Experience
There’s a growing demand among companies and research labs for scientific talent like yours. We’ll help you find the best career opportunities and get your name in front of the best employers. We’re Kelly Scientific Resources®, and our recruiters are degreed scientists who are actively involved in the scientific community and have a pulse on what's happening in the scientific job market. That means they know who’s hiring, when, and what skills are required, giving you the advantage you need in securing the right position, no matter what your discipline or field.
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