Summary
Overview
Work History
Education
Skills
Websites
Timeline
Generic

Branda Levchak

Summary

Detail-oriented professional specializing in clinical trial compliance and participant recruitment. Expertise in data verification and effective communication with sponsors, investigators, and regulatory bodies. Proven ability to manage patient information, laboratory samples, and compliance procedures across various clinical trials. Demonstrated success in enhancing trial procedures and ensuring data integrity through strong organizational and planning skills.

Overview

18
18
years of professional experience

Work History

Clinical Research Coordinator

Seattle Institute For Biomedical And Clinical Research
Seattle, Washington
09.2009 - Current
  • Led coordination of clinical trial activities to align with regulatory requirements.
  • Conducted device and drug clinical research within VA health care facilities.
  • Managed participant recruitment and screening processes for multiple studies efficiently.
  • Developed detailed study protocols while maintaining crucial documentation for trials.
  • Collaborated with multidisciplinary teams to ensure achievement of project goals.
  • Oversaw rigorous data collection, verification, and reporting procedures for research projects.
  • Facilitated effective communication among sponsors, investigators, and regulatory bodies.
  • Monitored patient safety during trials following established protocols.

Research Assistant

VA Puget Sound Health Care System
Seattle, Washington
03.2008 - 08.2009
  • Executed clinical research studies in VA health facilities, aligning with operational guidelines.
  • Enhanced efficiency by managing scheduling for interviews and participant follow-ups.
  • Identified suitable candidates through effective screening of potential study participants.
  • Extracted critical patient data from electronic health records for study use.
  • Ensured strict adherence to patient care protocols and clinical trial regulations.
  • Handled collection, processing, and delivery of trial participant specimens efficiently.
  • Worked alongside sponsors and investigators to ensure compliant research trials.
  • Recorded all activities related to clinical studies with accuracy.

Education

Associate Of Arts (AA) -

Highline College
Seattle, WA
01-2016

Skills

  • Clinical trial compliance
  • Protocol development
  • Data verification
  • Participant recruitment
  • Regulatory documentation
  • Project management
  • Phlebotomy and specimen handling
  • Good clinical practices
  • Informed consent

Timeline

Clinical Research Coordinator

Seattle Institute For Biomedical And Clinical Research
09.2009 - Current

Research Assistant

VA Puget Sound Health Care System
03.2008 - 08.2009

Associate Of Arts (AA) -

Highline College
Branda Levchak