
Clinical research professional with a Master’s degree in Microbiology & Immunology and an MBBS, with hands-on experience supporting IRB-approved human-subject research in academic medical settings. Experienced in participant recruitment, informed consent, protocol adherence, EMR-based chart review, biospecimen coordination, and regulatory documentation. Brings a strong foundation in molecular biology and translational research, with interest in supporting large-scale genomic and consortium-based studies. Seeking a Clinical Research Coordinator I role supporting genomic and translational research studies at Mount Sinai.
Clinical Research: Participant recruitment, informed consent, subject screening, enrollment support, scheduling coordination, chart review, protocol adherence, source documentation, biospecimen handling, safety documentation (AE/SAE support)
Regulatory & Compliance: IRB submissions support, regulatory documentation, GCP, HIPAA awareness
Data & Systems: EMR chart review, research databases, Microsoft Excel, Word, Outlook, PowerPoint; basic data analysis
Scientific & Analytical: Microbiology, immunology, RNA isolation, RT-PCR, qPCR, gel electrophoresis