Christiane Helmrich

Christiane Helmrich, PhD has extensive work experience in various roles related to quality assurance, clinical research, project management, and scientific analysis. Christiane has worked as the Head of Quality Assurance Product Development at medac GmbH since 2015. Previously, they served as the Associate Director of R&D GCP Quality Assurance at AbbVie Deutschland GmbH & Co. KG from 2012 to 2015, where they provided consultation and direction on quality assurance and GCP compliance.

From 2009 to 2012, Christiane worked at Abbott GmbH & Co. KG as the Associate Director of ICFO, managing a group responsible for global clinical study management. Christiane also represented the Clinical Field Operations perspective in headquarters and provided strategic input. In 2009, they briefly worked as a Freelancer in consultant clinical research.

Prior to that, Christiane held various roles at Synarc A/S, Kendle International, and Pharmalog Institut, where they gained experience in project management, clinical monitoring, and strategic planning. Christiane began their career as a Scientific Associate at the Laboratory for Mutagenicity Testing (LMP) and later served as the Deputy Manager of the Quality Assurance Unit and a part-time Study Manager at CCR GmbH & Co. KG and RCC Environmental Chemistry GmbH & Co.

Overall, Christiane Helmrich, PhD has a diverse background in the pharmaceutical and research industry, focusing on quality assurance and clinical research management throughout their career.

Christiane Helmrich, PhD pursued their education from 1981 to 1987 at Technische Universität Darmstadt. During this period, they acquired a Doctorate degree in Mathematics and Biology, specifically earning a Dr. rer. nat. degree.