I am a Medical Doctor with over 10 years of experience in oncology and clinical research, currently working as a Medical Monitor in international Phase 1–3 clinical trials.
I offer professional medical review services for clinical research projects, including patient eligibility assessment, clinical data review, safety evaluation, and protocol interpretation. I have extensive experience working with complex oncology cases, reviewing laboratory results, imaging, and medical histories to ensure compliance with study protocols and GCP requirements.
My services include:
- Patient eligibility assessment for clinical trials
- Medical review of clinical data and case reports
- Safety evaluation and adverse event review
- Protocol interpretation and clinical input
- Medical writing and scientific review
I collaborate with sponsors, CROs, and research teams worldwide and deliver clear, accurate, and actionable insights to support clinical decision-making.