
Detail-oriented biomedical science graduate with hands-on experience in toxicology and laboratory research, including study monitoring under OECD guidelines. Strong understanding of regulatory frameworks (REACH, CLP), data documentation, and laboratory techniques. Seeking an entry-level opportunity in clinical research to contribute to study coordination, patient safety, and regulatory compliance in clinical trials.
Study Monitoring (protocol compliance, data quality, timeline management, scientific writing)
Good Clinical Practice (GCP) – self-study, familiarity with ICH guidelines
Regulatory compliance
In-vivo and in-vitro testing
Data management
Laboratory analyses techniques
Communication and team collaboration
Time management