Clinical Research Coordinator

Taylor Vann

Washington, DC *****

************@*****.***

linkedin.com/in/taylorvanncra

240-***-****

PROFESSIONAL SUMMARY

Highly-motivated Clinical Research professional with experience in data management, protocol adherence and following good clinical practices. Well-versed in study protocols, standard operating procedures, and general clinical trials oversight. Industry background in healthcare; to include hospital, pharmaceutical, government, and public health organizations SUMMARY OF SKILLS AND CORE COMPETENCIES

• Data Management

• Data Verification

• Regulatory

Compliance

• Sponsor

Communications

• Essential

Documentation

• HIPAA Compliance

• Study Timepoint

Management

• SAE/AE Reporting

• Protocol Review

• Meditech/Cerner

EMR

• Microsoft Office

• Subject Enrollment

THERAPEUTIC AREAS

• Infectious Disease

• Oncology

• Neurology

PROFESSIONAL EXPERIENCE

Clinical Research Coordinator

February 2020 - present, National Institutes of Health, Washington, D.C.

• Assists physicians with data collection on patients seen by NIH Stroke Team

• Enters clinical research data into NIH database

• Manages data quality analysis and research projects

• Manages key study milestones such as screening, enrollment, and follow-ups

• Obtains informed consent from study participants

• Schedules and coordinates site study visits

• Completes case report forms and timepoint-specific study documents

• Supports the development and maintenance of site-specific Standard Operating Procedure documents

Patient Registration Specialist, Emergency Department July 2017 - February 2020, Frederick Memorial Hospital, Frederick, MD

• Greeted and checked incoming patients into the Meditech system; ambulatory and EMS

• Inputted patient demographic and insurance information in the Meditech system

• Responsible for verifying health insurance authorizations for inpatient and outpatient services.

• Collected and processed copayments

• Maintained hospital policies and procedures and HIPAA policies and procedures Patient Access Specialist (Intern)

September 2015 - July 2017, AstraZeneca, Gaithersburg, MD

• Performed intake of cases and document all relevant information in the AstraZeneca Access 360 Case Management system

• Provided administrative support to the managers and operations team

• Verified patient data with communication with the provider’s office, while maintaining HIPAA policies and procedures

• Ensured timely processing of support requests using decision tools and reference guides to determine appropriate case routing

• Assisted operations team with data quality projects and ensure that deadlines are met

• Monitored and documented productivity, quality and customer service standards. EDUCATION

Master of Public Health, Liberty University, expected completion July 2022 B.S. Health Services Management, University of Maryland University College, August 2018 CERTIFICATIONS

CPR/BLS for Healthcare Providers

Good Clinical Practice

Montreal Cognitive Assessment, MoCA

PROFESSIONAL AFFILIATIONS

Black Women in Clinical Research

The Association of Clinical Research Professionals Omega Nu Lambda National Honor Society

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