I am a Biochemical Engineer with hands-on experience in pharmacovigilance, regulatory support, and safety data management within international clinical and pharmaceutical environments. I have worked extensively with Individual Case Safety Reports (ICSRs), SAE/SUSAR case processing, MedDRA and WHO coding, and quality checks, ensuring full compliance with regulatory and data protection standards.
I am highly proficient in Oracle Argus and safety databases, report generation, data review, and client communication. Through my roles at global CROs, I have developed strong organizational, analytical, and documentation skills, as well as the ability to manage sensitive information with accuracy and discretion.
In addition to my technical background, I offer excellent communication skills and fluency in English and German, enabling me to support international clients with regulatory documentation, data management, administrative tasks, and customer or project support. I am detail-oriented, reliable, and comfortable working independently in remote and part-time settings.
I am currently interested in remote or freelance opportunities involving pharmacovigilance support, regulatory or clinical documentation, data entry and review, reporting, virtual assistance, and multilingual client communication.