Signe Lorentzen
About Signe Lorentzen
Signe Lorentzen is a Clinical Research Associate currently employed at TFS Trial Form Support in Copenhagen, Denmark. She has a master's degree from the University of Copenhagen and has previously worked at Novo Nordisk and Bispebjerg Hospital.
Work at TFS HealthScience
Signe Lorentzen has been employed at TFS Trial Form Support since 2019. In her role as a Clinical Research Associate, she is involved in various clinical trials and research projects. Her responsibilities include monitoring trial progress, ensuring compliance with regulatory requirements, and collaborating with study teams to facilitate successful outcomes. Her experience in this role spans over five years, contributing to her expertise in the clinical research field.
Previous Experience at Novo Nordisk
Signe Lorentzen worked at Novo Nordisk from 2014 to 2019. Initially, she served as a Clinical Safety Associate for three years, where she focused on patient safety and adverse event reporting. Following this role, she advanced to Senior Clinical Safety Associate, a position she held for two years. In these roles, she gained significant experience in clinical safety processes and regulatory compliance.
Background in Nursing
Before her career in clinical research, Signe Lorentzen worked as a Nurse Anesthetist and Intensive Care Nurse at Bispebjerg Hospital for two months in 2014. This experience provided her with a strong foundation in patient care and clinical procedures, which has been beneficial in her subsequent roles in clinical safety and research.
Education and Expertise
Signe Lorentzen studied at Københavns Universitet (University of Copenhagen), where she achieved her master's degree in 2017. Her educational background has equipped her with the knowledge and skills necessary for her roles in clinical research and safety, enhancing her contributions to the field.