Alexis Adams

China Grove,NC

Summary

Dedicated Clinical Research Coordinator known for productivity and efficiency in task completion. Skilled in patient recruitment, regulatory and protocol compliance, and data analysis to ensure smooth operation of clinical trials. Excels at communication, teamwork, and problem-solving, using these soft skills to navigate challenges and drive projects to completion. Always focused on advancing research goals with precision and integrity.

Overview

years of professional experience

Certification

Work History

Clinical Research Coordinator

Ora, Inc.

Andover, MA

05.2023 - Current

Coordinated 20 multicenter phase II and III trials for ophthalmic drugs, surpassing enrollment targets through block enrollment.
Supported site activation in Australia by assisting with screening visits and training site staff.
Maintained meticulous study documentation and regulatory files to ensure compliance.
Monitored protocol adherence, identified issues, and implemented corrective actions promptly.
Scheduled study visits and ensured timely communication with participants.
Managed data collection and organization using electronic data capture systems effectively.
Trained new staff on clinical trial procedures and best practices consistently.
Communicated with investigators, study staff, and sponsors throughout trial life cycle.

Science Teacher

Gaston County Schools

Dallas, NC

01.2022 - 05.2023

Designed engaging lesson plans catering to diverse learning styles.
Employed classroom technology to facilitate interactive learning experiences.
Executed hands-on experiments to deepen understanding of scientific concepts.
Collaborated with colleagues to ensure curriculum alignment across grade levels and subjects.
Monitored student progress and communicated achievements and areas for improvement to parents.

Education

Bachelor of Arts - Chemistry

University of North Carolina At Chapel Hill

Chapel Hill, NC

05-2021

Skills

Clinical Trial Management: Patient Recruitment, Patient Screening & Enrollment, Informed Consent, Data Collection, Data Integrity
Data Management: EDC Systems, Medidata, Oracle Clinical, Veeva Vault, ClinCapture

Regulatory Compliance: Good Clinical Practice (GCP), FDA Regulations, ICH Guidelines, Informed Consent Procedures, HIPAA Regulations, Adverse Event Reporting
Technical Skills: Microsoft Suite (Excel, Word, Outlook), Data Entry, Quality Control