Franziska Oldenburg
About Franziska Oldenburg
Franziska Oldenburg is a Medical Safety Manager and Medical Review Lead at Novocure in Root, Lucerne, Switzerland, with extensive experience in medical safety, pharmacology, and regulatory compliance.
Company
Franziska Oldenburg currently works at Novocure in Root, Lucerne, Switzerland. Her role at Novocure includes serving as the Medical Safety Manager - Medical Review Lead. Previously, she served in various capacities at Novocure, including as Medical Safety Specialist and Medical Safety Associate.
Title
Franziska Oldenburg holds the title of Medical Safety Manager - Medical Review Lead. She has also been associated with Novocure as a Medical Safety Specialist and Medical Safety Associate. Her titles reflect her increasing responsibility and involvement in medical safety and review processes.
Education and Expertise
Franziska Oldenburg studied at Charité Berlin, achieving Promotionsstudentin status. She also attended Celtis-Gymnasium, where she completed her Abitur from 2000 to 2012. Afterward, she studied Pharmazie at Ludwig-Maximilians-Universität München, earning her Staatsexamen. Her educational background has equipped her with extensive knowledge in pharmacy, medical device regulations, and drug discovery.
Background
Franziska Oldenburg has accumulated a diverse professional background. Before her current role, she worked as a Pharmacist at Apotheke Am Guardinipark, a Medical Safety Specialist and Medical Safety Associate at Novocure, and held several internship roles in community pharmacy and pharmaceutical marketing. Her career also includes experience in drug discovery and development, and manufacturing and support at Takeda.
Achievements
In her current role at Novocure, Franziska Oldenburg provides MedDRA coding guidance for the global complaint handling team, handles coding reconciliation within the Medical Safety team, supports the creation of Periodic Safety Update Reports (PSUR) and Post-Market Clinical Follow-up Reports (PMCFR), and conducts literature reviews. Additionally, she trains the Medical Safety team and other departments, showcasing her extensive knowledge of EU Medical Device Regulation (MDR) and international guidelines.