
Clinical research–focused healthcare professional with a B.S. in Biochemistry and hands-on experience in patient care, laboratory operations, and healthcare documentation. Skilled in coordinating patient interactions, maintaining regulatory compliance, and supporting multidisciplinary medical teams. Experienced in specimen handling, EMR documentation, and adherence to clinical protocols. Highly organized, detail-oriented, and motivated to contribute to oncology clinical trials through patient-centered coordination and data integrity
Clinical Trial Support
Patient Coordination & Education
Informed Consent Support
EMR & Medical Documentation
Specimen Handling & Processing
Regulatory Compliance (HIPAA, SOP adherence)
Data Entry & Record Accuracy
Interdisciplinary Team Collaboration
Time Management & Organization