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Clinical Research Coordinator

Location:
Birmingham, AL
Posted:
October 27, 2025

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Resume:

S K I L L S

Self Motivation

Research & Strategy

Response monitoring

Outreach Programs

Customer Service

Workflow Evaluation Customer

Service

Effective Time Management

Conflict Resolution

Problem solving

Leadership and teamwork

Critical thinking and problem

solving

Fast Learner

OJOSIDE AGBALI

S U M M A R Y

Professional Clinical Research Coordinator with 15+ years of experience in clinical research, clinical trials, and regulatory compliance. Proficient in developing, coordinating, and executing clinical research protocols. Skilled in data collection and analysis, monitoring of clinical trials, and reporting of results. .

WORK E X P E R I E N C E

Senior Clinical Research Coordinator

Joseph M Still Burn Center

Dec 2024 - Jul 2025

Augusta, GA

Coordinated the recruitment, scheduling, and enrollment of participants in clinical research studies.

Developed and maintained clinical research databases. Monitored patient safety during clinical trials.

Developed and implemented strategies to ensure ethical conduct of research studies. Developed and maintained participant records and regulatory documents for clinical trials. Managed the collection and analysis of clinical data. Worked with sponsors and other stakeholders to ensure compliance with study protocols. Developed and maintained research protocols and procedures. Developed and maintained study resources such as patient information sheets. Participated in the design and implementation of research studies. Prepared protocols, informed consent forms, and other regulatory documents. Site Manager/Senior Clinical Research Coordinator Oct 2022 - Nov 2024 Tilda Research Birmingham, AL

Supervised and coordinated the work of contractors and subcontractors to ensure compliance with safety regulations and project timelines Developed a research database to store and organize data from the research project

Coordinated clinical trials with multiple sites, ensuring timely completion of study deliverables

Developed and implemented study protocols that adhere to FDA regulations and Good Clinical Practice guidelines

Managed study supplies and pharmacy operations, ensuring compliance with regulations

Monitored study progress and data quality, identifying and resolving issues in a timely manner

Developed and maintained positive working relationships with study participants and healthcare providers

Collected, analyzed, and reported data in accordance with study protocols and industry standards

Developed and implemented processes to ensure compliance with study protocols and SOPs

Developed recruitment strategies to ensure adequate enrollment of study participants

Clincal Research Case Manager(Contract) Oct 2021 - Aug 2022 Insight Global Atlanta, GA

Entered patient data into data systems, answered queries, maintained research Reviewed weekly inventory charts and recorded facility needs, accordingly. 404-***-****

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

Birmingham, AL 35040

Maintained and ensured spa utilities met corporate standards and operating procedures. Documents, and performed assigned duties.

Applied therapeutic interventions tailored to research protocols, including patient education, crisis intervention, and emotional support. Utilized motivational interviewing techniques to improve patient compliance with clinical trial protocols and health objectives. Collaborated with multidisciplinary teams to address patient-specific needs and improve outcomes.

Provided support to clinical research teams throughout the drug development process Clinical Research Coordinator(Contract) May 2021 - Oct 2021 Sleep Practitioners Macon, GA

Collected, analyzed, and maintained research data while adhering to protocols for subject appointments, documentation, and data entry. Medical Terminology

Ability to Work Under Pressure

CTMS

Good Clinical Practice

Communication Skills

Microsoft Office

Participated actively in meetings and conferences to streamline research operations.

Provided therapeutic support by educating patients on treatment plans, ensuring protocol adherence, and addressing patient concerns. Assisted in patient care, including escorting patients to exam rooms, obtaining vital signs, and verifying chart accuracy.

Clinical Research Coordinator/Medical Assistant Oct 2020 - May 2021 Gastroenterology Associates of Central Georgia Macon, GA Drew blood, monitored vital signs, administered injections, and prepared lab specimens for analysis.

Educated patients by providing medication and diagnosis information, offering therapeutic guidance, and supporting mental and emotional well-being. Coordinated research-related activities, including accurate data entry, protocol adherence, and subject monitoring.

Delivered excellent customer service, answered multi-line telephones, and ensured smooth clinical and research operations.

Certified Medical Assistant (CMA) Apr 2019 - Jan 2020 Allergy Asthma and Sinus Center Macon, GA

Conducted patient intake, administered injections, and provided allergy/immunotherapy treatments.

Monitored and documented patient vitals and reactions, ensuring accurate record-keeping and compliance with protocols.

Assessed patient needs and managed post-injection observation periods to promptly address any adverse reactions.

Maintained treatment room cleanliness and ensured availability of supplies while adhering to OSHA guidelines.

Certified Medical Assistant (CMA) Oct 2018 - May 2019 Quadmed Macon, GA

Performed clinical tasks including phlebotomy, vital signs monitoring, injections, ECGs, and spirometry tests.

Accurately documented patient information and supported providers during procedures and consultations.

Managed offce supplies, monitored freezer and refrigerator temperatures, and ensured timely medication orders for the clinic.

Delivered excellent customer service by addressing inquiries and directing calls via multi-line telephone systems.

Clinical Research Coordinator May 2014 - Oct 2018

University of Alabama Birmingham Birmingham, AL

Scheduled and conducted clinical research tasks, including vital signs monitoring, ECGs, injections, and lab sample collection/processing. Maintained participant records, managed study documentation, and ensured adherence to protocols.

Assisted with reporting, participant compensation processing, and study-related administrative duties.

Collaborated with research teams and participated in study meetings to support project outcomes.

Recruited patients for research studies, Drew blood, monitored vital signs, gave injections, performed ECGs, entered patient information in the computer, assisted nurses as needed, answered multi-line telephones and directed calls and provided good customer service

E D U C ATION

Bachelor of Science : Health Science May 2023

Southern New Hampshire University, Manchester, NH

Associate of Applied Science: Medical Assistant Jan 2003 Virginia College, Homewood, AL



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