Berufsperspektiven Launching Your Career in Clinical Research: Entry-Level Roles and Future Opportunities for Graduates
In this presentation, Dr. Richter will provide an overview of the different phases of drug development and clinical research. She will explain how clinical trials are conducted, highlighting the key departments involved and their respective responsibilities. Additionally, Dr. Richter will delve into the critical role of drug safety in both individual clinical trials and the broader drug development process. The presentation will conclude with an overview of current job opportunities in Germany within the clinical research field.
Bio
Dr. rer. nat. Sabine Richter has dedicated over three decades to the clinical research industry. She began her career as a Clinical Research Associate (CRA) in the pharmaceutical industry before transitioning to Clinical Research Organizations (CROs). Throughout her tenure at CROs, Dr. Richter held diverse roles in project management, clinical operations, training, compliance, business development, and pharmacovigilance. Her expertise in pharmacovigilance also extended to leading a team of biostatisticians and programmers specialized in integrated safety analyses.
From 2018 until the end of the program in 2023, Dr. Richter served as an Associate Lecturer in Pharmaceutical Medicine at the University of Duisburg-Essen, Ruhr Campus Academy gGmbH. In this role, she taught the Drug Safety Study Unit and contributed to the final examinations of MSc students.
Overview
Table
Date | Wednesday, 13 November, 2024 |
Time | 18:30 |
Location | Hörsaalzentrum Chemie, Im Neuenheimer Feld 252, 69120 Heidelberg |
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Registration for 'Launching Your Career in Clinical Research'
In case of any issues with registration: simone.lasser@uni-heidelberg.de