The Research Compliance Analyst uses advanced research compliance concepts to interpret highly complex and broad regulations, policies and guidelines. Provides advice and counsel regarding computerized quality management systems (QMS), related data integrity concerns, and related processes as they may relate to Food & Drug Administration (FDA), Good Clinical Practice (GCP) and other health authority-regulated business. Facilitates plan to meet these standards. Helps prepare documentation and database for audit when needed. Regularly works on highly complex research compliance issues where analysis requires an in-depth evaluation of variable factors. Exercises judgment in selecting methods, techniques and evaluation criteria to anticipate and identify problems and develop and implement
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