Clinical Research Coordinator - Full-time

Benefits

Qualifications

• •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
• •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
• •9 more items(s)

Responsibilities

• •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
• •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
• •13 more items(s)