Clinical Research Coordinator - Full-time
Behavioral Health Market Context
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Benefits
Competitive salaryHealth, dental & vision benefitsPaid time off & paid holidaysProfessional development and certification supportGrowth opportunities within ADF Medical ServicesCompetitive salaryHealth, dental & vision benefitsPaid time off & paid holidaysProfessional development and certification supportGrowth opportunities within ADF Medical Services7 more items(s)
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)