MD- and PhD-trained clinical research professional with extensive experience in oncology and translational research. Skilled at coordinating protocol-driven activities, ensuring data quality, and supporting regulatory compliance. Committed to enhancing clinical operations through effective collaboration and meticulous study documentation.
Work History
Postdoctoral Fellow
University of Maryland, Baltimore
Baltimore
Collaborated with principal investigators and multidisciplinary research teams supporting protocol-driven translational oncology studies.
Coordinated study documentation, protocol implementation, research data collection, scientific reporting, and study workflows while ensuring data quality and regulatory compliance.
Maintained accurate research records, supported quality assurance activities, and facilitated communication across research teams to ensure timely study execution.
Postdoctoral Associate
Hillman Cancer Center, University of Pittsburgh
Pittsburgh
Supported protocol-driven oncology research through study documentation, biospecimen coordination, research data management, and multidisciplinary collaboration.
Coordinated activities among investigators, pathology personnel, IRB stakeholders, hospital staff, logistics teams, and patient families to support implementation of the Lung Rapid Autopsy Program.
Contributed to standardized protocol execution, biospecimen collection, documentation accuracy, and regulatory compliance within a complex translational research environment.
Conducted participant screening and clinical assessments in accordance with standardized protocols while maintaining accurate documentation and regulatory compliance.
Educated participants regarding required procedures and collaborated with multidisciplinary healthcare teams to support efficient clinical workflows and participant-centered care.
Education
Project Management Institute
Penn, PA
01-2024
Ph.D. - Biomedical Sciences
The University of Tokyo
Japan
04-2020
M.D. - Medicine
Kilimanjaro Christian Medical University College
Tanzania
11-2012
Skills
Clinical Trial Operations Support
Clinical Research Coordination
Protocol Implementation
ICH-GCP Compliance
Study Documentation
Regulatory Documentation
Human Subjects Research
Participant Screening
Research Data Collection
Data Quality Assurance
Biospecimen Coordination
Cross-functional Collaboration
Scientific Documentation
Medical Terminology
Microsoft Office Suite
Training
Project Management Institute (PMI) Training
Personal Information
Immigration Status: Lawful Permanent Resident
Title: Clinical Research Professional | Physician-Scientist
Work Permit: Authorized to Work in the United States
Postdoctoral Fellow at Regeneron Genetic Center, Regeneron Pharmaceuticals, Inc.Postdoctoral Fellow at Regeneron Genetic Center, Regeneron Pharmaceuticals, Inc.