Description

Helping pharma, MedTech, and diagnostic teams navigate clinical trials and EU regulations with confidence. With a background in clinical pharmacology and hands-on experience in CTIS, EU MDR, and protocol writing, I connect the dots between science, strategy, and operations.

Whether it’s preparing regulatory submissions, designing trial protocols, or shaping early-phase study plans, I bring structure to complex processes. Surely, always with a focus on what works in the real world.

Industry field of expertise

Languages

German
Fluent
English
Fluent

Workplace preferences

Remote only

Primarily works remotely

Clinical Pharmacology Department of University Hospital Heidelberg
Medical Doctor
PHARMACEUTICALS INDUSTRY
February 2024 - Today (2 years and 4 months)
Clinical Pharmacology resident, deeply involved in industry and investigator initiated clinical trials, study set-up and conduct, science regulatory.
BioMex GmbH
Deputy Center Manager and Digital Transformation Advisor
September 2022 - December 2024 (2 years and 3 months)
69 Heidelberg, Germany
Led trial operations and biological material (plasma, leukopak) workflows;
Product Owner for ERP development tailored to company’s research and regulatory needs.
Product & Process Optimization Life Science Business development
Neurology Department of RoMed Kliniken
Medical Doctor
October 2020 - July 2022 (1 year and 9 months)
Rosenheim, BY, Germany
Resident doctor in neurology department