Program Manager, Yale Reproductive Sciences Biobank at Yale University School of Medicine (2024-01 – Present)
- Direct scientific and operational activities for a multi-investigator reproductive sciences biobank supporting concurrent investigator-initiated, industry-sponsored, and foundation-sponsored translational research programs in reproductive health.
- Develop research protocols and informed consent materials and oversee IRB-governed workflows for participant consent, clinical data abstraction, biospecimen annotation, privacy protection, and quality control, ensuring research data and biospecimens remain accurate, traceable, compliant, and fit for scientific use.
- Coordinate Material Transfer Agreements (MTAs), Data Use Agreements (DUAs), and External Sponsored Agreement Process (ESAP) reviews for academic and industry collaborations, facilitating compliant transfer of biospecimens and associated research data.
- Coordinate investigators, clinical teams, laboratory personnel, and institutional partners across multiple projects, establishing priorities, monitoring milestones, identifying risks, and maintaining progress toward research, publication, and presentation deadlines.
- Develop publication and congress deliverables - including manuscripts, structured abstracts, scientific figures, and presentations, by integrating molecular, clinical, bioinformatic, and statistical findings into tailored to journal peer review, congress formats, and investigator-facing briefings.
- Review scientific outputs for evidentiary support, data consistency, methodological accuracy, and alignment with study objectives before submission to journals, scientific meetings, or institutional reviewers.
Postdoctoral Clinical Research Associate, Pulmonary, Critical Care & Sleep Medicine at Yale University School of Medicine (2022-01 – 2024-12)
- Concurrently coordinated eight multinational Phase 2-3 industry-sponsored clinical trials across large pharmaceutical and biotech sponsors including companies across the IPF, pulmonary, and critical care therapeutic landscape, serving as the primary site-level point of contact for sponsor CRAs and monitors.
- Ensured ICH-GCP-compliant site operations across all active protocols, including source document verification, EDC data entry and query resolution, informed consent procedures, and protocol deviation documentation.
- Prepared and represented the site during sponsor monitoring visits and regulatory audits, maintaining inspection-ready trial master files, source records, and regulatory binders with zero critical findings.
- Completed SAE/AE identification, documentation, and direct reporting into sponsor safety systems in alignment with protocol-defined timelines and regulatory requirements.
- Supported IRB submissions and amendments, site initiation activities across new and ongoing studies, translating sponsor requirements into executable site-level workflows.
- Analyzed study findings and synthesized published evidence to support interpretation of experimental and clinical results, contributing to peer-reviewed manuscripts and multidisciplinary scientific presentations.
Resident Physician, Internal Medicine at Belarusian State Medical University (2020-01 – 2021-12)
- Delivered evidence-based inpatient and outpatient care for adults with diverse acute and chronic medical conditions in collaboration with multidisciplinary specialist teams.
- Rapidly evaluated emerging clinical evidence during the COVID-19 pandemic and contributed to national clinical guidance by translating evolving research into precise, clinically actionable recommendations.
