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Responsible for quality review of safety reports, compiling quality metrics, supporting audits, and assisting in drug safety data management processes.

The QA Controlled Docs Associate manages controlled documents, ensures compliance, tracks metrics, participates in process improvements, and trains others.

The role involves programming using Medidata Rave and SAS, developing datasets, and creating reporting specifications while managing multiple projects and ensuring compliance with quality standards.

Lead preparation and review of safety reports, manage report writing teams, ensure quality deliverables, and foster client relationships in a pharmaceutical context.

This role leads the strategy and development of data management software for the life sciences sector, managing from conception to launch and ensuring compliance with industry standards.