Oncology MD supporting clinical trials with expert medical review, safety evaluation, and patient eligibility assessment for accurate, compliant, and reliable decisions.
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 have extensive expertise in patient eligibility assessment, safety evaluation, clinical data review, and protocol interpretation across complex oncology studies.
I collaborate with sponsors, CROs, and investigators in multicenter global trials, ensuring high-quality study conduct and compliance with GCP and regulatory requirements. My work includes reviewing medical records, laboratory data, imaging, and adverse events, as well as supporting clinical decision-making in high-risk patient populations.
I provide services in medical review, clinical research support, medical writing, second opinions, and scientific consulting. I am particularly experienced in translating complex clinical information into clear, structured, and actionable insights.
My approach is detail-oriented, reliable, and aligned with regulatory expectations, with a strong focus on accuracy and clarity in all deliverables.
Work Terms
Available for remote projects with flexible hours (typically 10–20 hours/week, depending on scope). Open to both short-term and ongoing collaborations.
Communication via Freelancer messaging and scheduled calls within the platform. I aim to respond promptly and maintain clear, structured communication throughout the project.
Work is delivered with a strong focus on accuracy, clarity, and adherence to agreed timelines. I am comfortable working with confidential medical data and follow strict professional and ethical standards.
Hourly and fixed-price projects are both welcome.