Molecular biology graduate with hands-on training in GMP, GCP, and QC standards. Strong academic foundation in laboratory techniques and a commitment to excellence in pharmaceutical and biotech environments. Actively seeking roles in clinical research to leverage skills and contribute to regulated scientific settings. Proficient in English and certified in Danish (FVU4).
Clinical research design and ICH-GCP
Informed consent and GMP documentation
Pharmaceutical quality control
PCR and spectrophotometry
Cleanroom compliance
Clinical data analysis
Microsoft Excel proficiency
Attention to detail
Team collaboration
Scientific writing
- Clinical Trials Operations Specialization
- Design and Interpretation of Clinical Trials – Coursera, June2025
- Clinical Trials Operations Specialization – Coursera, June2025
- QC.Quality Control for Medical & Pharmaceutical Production
U/NORD, May 2025
- Introduction to Industrial Bioprocess Development – Coursera, May 2025
- GLP(Good Laboratory Practice) – Pharma lesson(Verified), May 2025
- Injection Techniques (Vaccination & IM/SC) – LabVikar, Apr 2025
- Data Management for Clinical Research – Coursera, Apr 2025
- GCP(Good Clinical Practice Specialization) – Coursera, Apr 2025
- GMP (Good Manufacturing Practice)(Theoretical) – LabVikar, Mar 2025
- FVU4 Danish language, Feb2025
- Essential Lab Skills – IAU Tehran, Feb 2020