Brooklyn Culton
Dallas
Summary
As a Research Coordinator, I have gained experience in regulatory affairs, experimental design, and data management, contributing to research integrity and compliance at the University of Arkansas for Medical Sciences and the University of Arkansas at Pine Bluff. I have developed strong skills in documentation, problem-solving, and team collaboration, ensuring studies run smoothly while engaging effectively with participants and research teams. While I bring a solid foundation in clinical research, I am eager to continue growing, refining my expertise, and expanding my contributions to research operations and regulatory processes. With a strong willingness to learn, adaptability, and excellent communication skills, I am excited to take on new challenges and further develop in the field.
Overview
2
2
years of professional experience
1
1
Certification
Work History
Research Coordinator /Regulatory Specialist
University Of Arkansas At Pine Bluff
08.2021 - 05.2022
- Ensured compliance with regulatory standards by maintaining and organizing essential study documents, supporting IRB submissions, and facilitating adherence to institutional protocols and ICH-GCP guidelines.
- Served as the primary liaison between research teams, investigators, and study staff, ensuring timely resolution of study-related inquiries and protocol clarifications via email and phone; supported regulatory documentation processes by maintaining accurate study records and facilitating compliance with institutional guidelines.
- Organized and maintained study-related documents by filing, scanning, mailing, and emailing materials, ensuring accurate record-keeping and compliance with institutional protocols; facilitated document tracking and supported communication between research teams, sponsors, and investigators.
- Maintained and updated regulatory documentation, including site logs such as participant visit logs and adverse event logs, ensuring accurate record-keeping and compliance with institutional protocols.
- Conducted routine reviews to identify discrepancies, collaborated with Principal Investigators to resolve issues, and implemented corrective actions to uphold study integrity.
- Implemented quality control measures by temporarily pausing pre-approved study protocols to facilitate additional review, ensuring meticulous adherence to protocol compliance standards under the supervision of the Principal Investigator.
- Eager to develop expertise in inventory management by learning to track, order, and maintain research supplies and equipment in alignment with institutional procedures and study needs. Committed to ensuring proper equipment functionality and supporting research operations efficiently.
- Compiled, documented, and maintained study-related data to ensure accurate formatting and accessibility for investigators and regulatory review. Supported compliance efforts by organizing essential documents in accordance with institutional protocols and regulatory requirements.
- Updated and maintained participant databases (Google Sheets, Microsoft Excel, or other tracking systems), ensuring real-time accuracy in study enrollment records.
Research Coordinator
University of Arkansas for Medical Sciences, UAMS
06.2020 - 05.2021
- Maintained effective and positive communication with research participants, investigators, sponsors, and team members to support collaboration and regulatory compliance.
- Facilitated accurate documentation and adherence to study protocols, contributing to a professional and well-coordinated research environment."
- Assisted in participant identification, recruitment, and pre-screening through phone screenings and database review, ensuring compliance with study eligibility criteria.
- Maintained accurate records of recruitment efforts for regulatory tracking and adherence to institutional protocols.
- Assisted in coordinating and scheduling participant study visits while maintaining accurate records to support regulatory compliance.
- Sent study reminders to facilitate participant retention and adherence to study protocols.
- Supported participant identification, recruitment, and pre-screening through phone screenings and database review, ensuring adherence to study eligibility criteria. Maintained detailed recruitment records to facilitate regulatory tracking and compliance with institutional protocols.
- Conducted meticulous participant qualification by re-verifying eligibility criteria with participants and verified participant eligibility by thoroughly reviewing participant records, study charts, and subject databases in alignment with study protocols.
- Ensured accurate documentation of eligibility checks and maintained adherence to study inclusion and exclusion criteria, contributing to the integrity and validity of research data.
Education
Bachelor of Science - Psychology
University of Arkansas At Pine Bluff
Pine Bluff, AR05-2022
High School Diploma -
Cedar Hill Highschool
Cedar Hill, TX05-2018
Skills
- Experimental Design
- Data Organization
- Professional Communication & Collaborative
- Technical & Analytical Skills
- Research Management
- Participant & Team Centered Engagement
- Independent & Self Motivated
- Data & Documentation Management
- Positive & Professional Attitude
Certification
- CITI Training
Timeline
Research Coordinator /Regulatory Specialist
University Of Arkansas At Pine Bluff
08.2021 - 05.2022
Research Coordinator
University of Arkansas for Medical Sciences, UAMS
06.2020 - 05.2021
- CITI Training
Bachelor of Science - Psychology
University of Arkansas At Pine Bluff
High School Diploma -
Cedar Hill Highschool
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