Susanne Nielsen
About Susanne Nielsen
Susanne Nielsen is a Clinical Research Associate with extensive experience in clinical research and safety. She has worked at TFS Trial Form Support since 2016 and has held various roles at Novo Nordisk and other healthcare institutions over the past several years.
Work at TFS HealthScience
Susanne Nielsen has been employed at TFS Trial Form Support since 2016, serving as a Clinical Research Associate. In this role, she is involved in various clinical trials, ensuring compliance with regulatory standards and facilitating the research process. Her experience at TFS spans over eight years, contributing to her expertise in clinical research methodologies and practices.
Previous Experience at Novo Nordisk
Before her current role at TFS, Susanne Nielsen worked at Novo Nordisk as a Clinical Safety Associate from 2015 to 2016. During her tenure of one year, she was responsible for monitoring clinical trial safety data and ensuring adherence to safety regulations. Additionally, she has been employed at Novo Nordisk as a Laborant since 2011, accumulating over 13 years of experience in this position.
Background in Clinical Research Coordination
Susanne Nielsen has a background in clinical research coordination, having worked as a Study Coordinator at Rigshospitalet from 2013 to 2015 for two years. In this role, she coordinated various clinical studies, managing participant recruitment and data collection processes. This experience has enhanced her skills in project management and collaboration within clinical research settings.
Early Career as a Nurse
Susanne Nielsen began her career in healthcare as a Nurse at Hvidovre Hospital, where she worked for seven months in 1990 to 1991. This early experience in patient care provided her with a foundational understanding of clinical environments and patient interactions, which has informed her subsequent roles in clinical research.