Clinical Research Coordinator
ADF Medical, Westlake, OH, United States
ADF Medical Services Inc.
We're looking for a motivated and detail-driven
Clinical Research Coordinator
to support our clinical trials and research initiatives. If you have a passion for healthcare research and strong organizational skills — we'd love to have you on our team.
What You’ll Do:
Coordinate and oversee day-to-day clinical trial activities and research protocols
Recruit, screen, and enroll eligible study participants
Collect, record, and maintain accurate research data and patient records
Ensure all research activities comply with FDA regulations, GCP guidelines, and IRB requirements
Communicate with sponsors, investigators, and regulatory agencies
Prepare and submit regulatory documents and research reports
Monitor participant safety and report adverse events promptly
Train and support research staff on study protocols and procedures
Requirements:
Bachelor's degree in Life Sciences, Nursing, Healthcare, or a related field
2+ years of experience in clinical research or a related role
Knowledge of FDA regulations, GCP, and IRB submission processes
Strong data management and documentation skills
Excellent organizational and time management abilities
SOCRA or ACRP certification is a strong plus
Benefits:
Experience with Electronic Data Capture (EDC) systems is preferred
Competitive salary
Health, dental & vision benefits
Paid time off & paid holidays
Professional development and certification support
Growth opportunities within ADF Medical Services
#J-18808-Ljbffr
We're looking for a motivated and detail-driven
Clinical Research Coordinator
to support our clinical trials and research initiatives. If you have a passion for healthcare research and strong organizational skills — we'd love to have you on our team.
What You’ll Do:
Coordinate and oversee day-to-day clinical trial activities and research protocols
Recruit, screen, and enroll eligible study participants
Collect, record, and maintain accurate research data and patient records
Ensure all research activities comply with FDA regulations, GCP guidelines, and IRB requirements
Communicate with sponsors, investigators, and regulatory agencies
Prepare and submit regulatory documents and research reports
Monitor participant safety and report adverse events promptly
Train and support research staff on study protocols and procedures
Requirements:
Bachelor's degree in Life Sciences, Nursing, Healthcare, or a related field
2+ years of experience in clinical research or a related role
Knowledge of FDA regulations, GCP, and IRB submission processes
Strong data management and documentation skills
Excellent organizational and time management abilities
SOCRA or ACRP certification is a strong plus
Benefits:
Experience with Electronic Data Capture (EDC) systems is preferred
Competitive salary
Health, dental & vision benefits
Paid time off & paid holidays
Professional development and certification support
Growth opportunities within ADF Medical Services
#J-18808-Ljbffr