Anneli Thorgren

Anneli Thorgren

Drug Safety Officer @ TFS HealthScience

About Anneli Thorgren

Anneli Thorgren is a Drug Safety Officer at TFS Trial Form Support in Lund, Sweden, where she has worked since 2015. She has a diverse background in patient safety and midwifery, with previous roles at AstraZeneca and Region Skåne.

Work at TFS HealthScience

Anneli Thorgren has served as a Drug Safety Officer at TFS Trial Form Support since 2015. In this role, she is responsible for monitoring and ensuring the safety of pharmaceutical products. Her tenure at TFS spans over nine years, during which she has contributed to various drug safety initiatives. The organization is known for its commitment to clinical research and regulatory compliance, and Thorgren's expertise plays a vital role in maintaining these standards.

Education and Expertise

Anneli Thorgren has pursued education in several institutions. She studied at Uppsala University in 2015 and at Malmö University in 2009. Additionally, she attended Lund University from 2005 to 2007 and again in 2012. Thorgren also completed a two-year program at Sophiahemmet University College from 1991 to 1993. Her educational background supports her expertise in drug safety and patient care.

Background in Healthcare

Prior to her current role, Anneli Thorgren worked in various healthcare positions. She served as a Leg Barnmorska at Region Skåne from 2007 to 2015, where she provided midwifery services. Additionally, she worked as a Patient Safety Specialist at AstraZeneca from 1999 to 2007 and at Proffice from 2009 to 2010. Her experience in these roles has equipped her with a strong foundation in patient safety and healthcare practices.

Previous Roles and Experience

Anneli Thorgren has held multiple positions throughout her career. She worked as a Medical Writer at TFS Trial Form Support for three months in 2007. Her experience also includes a role as a Patient Safety Specialist at Proffice for nine months in 2009. These positions have contributed to her comprehensive understanding of drug safety and regulatory processes.

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