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US-MD-Rockville: Research - Biotech

Date: 11-Sep-2012
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Research - Clinical Trials

Responsibilities include providing assistance toward the development and formatting of documents;

assisting in document control processes such as coordination of SOPs, work instructions, and project plan development;

and training project staff on quality assurance-related activities specifically focusing on the quality of written documents.

The QA associate will also conduct reviews of project deliverables, work instructions, and other project documentation as required. Qualified candidates must be detail oriented and possess strong organizational, time-management, interpersonal, problem-solving, and written communication skills. Strong computer skills are a must. Experience working on Government-funded clinical trials is a plus.

A bachelorís degree in science, nursing, social science, information systems, or other health-related field, with at least 2 years of experience within quality assurance in the pharmaceutical, biotech, or clinical research industry is required.

To apply for this position, please visit this Website.

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