Open to opportunities

Francesca McKay

@francescamckay

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Clinical Research Coordinator dedicated to advancing medical research.

United States

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What I'm looking for

I seek a collaborative environment that fosters innovation and growth in clinical research.

As a Clinical Research Coordinator with extensive experience in managing clinical trials, I have developed a strong foundation in recruitment strategies, regulatory compliance, and patient engagement. My role at the Clinical Trials Center of Middle Tennessee has allowed me to coordinate multiple studies, ensuring adherence to IRB requirements while maintaining high standards of patient care.

Throughout my career, I have successfully increased study engagement and streamlined processes, contributing to the timely completion of research objectives. My background in public health and psychological sciences equips me with a unique perspective on patient interactions and data management, making me a valuable asset to any research team.

Experience

Work history, roles, and key accomplishments

Current

Clinical Research Coordinator

Current

Clinical Trials Center of Middle Tennessee

Feb 2024 - Present (1 year 4 months)

Collaborated with the Principal Investigator to develop and implement recruitment strategies, ensuring compliance with IRB requirements. Conducted procedural aspects of studies, including informed consent, subject screening, and coordination of participant tests, while meticulously documenting adverse events and completing Case Report Forms. Maintained comprehensive study records and facilitated m

Recruitment Strategy Informed Consent Forms Data Collection Quality Assurance Compliance With Study Protocols

Clinical Research Coordinator I/II

Vanderbilt University Medical Center

Oct 2022 - Mar 2024 (1 year 5 months)

Maintained compliance with ICH-GCP Guidelines, regulatory requirements, and SOPs while coordinating clinical assessments for autonomic dysfunction studies. Managed participant selection, consent, screening, and education, significantly increasing study engagement and contributing valuable data to investigator meetings. Oversaw regulatory document maintenance and trained an undergraduate research a

ICH GCP Regulatory Compliance Clinical Assessment Researchmatch Data Analysis Training

Research Assistant

University of Arizona (Banner - University Medical Center Tu

Jul 2018 - May 2019 (10 months)

Recruited qualified participants through phone interviews and screens, managing participant visits, debriefing, and data entry via REDCap. Responsible for designing and implementing a participant outreach program. Provided assistance with grant writing revisions.

REDCap Data Entry Interviewing Data Management

Education

Degrees, certifications, and relevant coursework

University of Arizona

Master of Public Health, Public Health

Completed a Master of Public Health program, focusing on public health principles and practices. Gained expertise in epidemiology, biostatistics, and health policy.

University of Arizona

Bachelor of Science, Psychological Sciences

Obtained a Bachelor of Science in Psychological Sciences. Developed a strong foundation in psychological theories, research methods, and data analysis.