Remote Clinical Research Coordinator II – Neurology

Emory University; Atlanta (GA); Hybride; USD 60 000 - 90 000; Plein temps

Résumé du poste

Emory University in Atlanta, GA is seeking a Clinical Research Coordinator II responsible for administrating clinical trial activities, managing study data and assisting with regulatory submissions.

The role requires evaluating participant eligibility, coordinating procedures, and ensuring protocol adherence while mentoring staff and supporting recruitment efforts. Remote work is possible with in-person campus commute as needed.

Qualifications

• High School Diploma or GED with five years clinical research experience.
• Two years of college in a science/health/business program with three years clinical research experience.
• LPN license with two years clinical research experience.
• Bachelor's degree in science/health/business with one year clinical research experience.
• Master's/MD/PhD in a related program.

Responsabilités

• Manage databases, flow sheets, source documents and CRFs.
• Guide less experienced staff and coordinate team effort.
• Screen participants, determine eligibility and obtain consent per protocol.
• Approve orders for supplies and maintenance of equipment.
• Develop recruitment strategies and conduct participant screenings.
• Supervise collection and processing of study specimens.
• Coordinate scheduling and charging for procedures and services.
• Ensure protocol compliance and audit source documents; attend sponsor meetings.
• Prepare regulatory submissions and related documentation.
• With credentialing, may perform phlebotomy or diagnostics.
• Perform other approved responsibilities as needed.

Connaissances

Clinical research coordination

Regulatory compliance

Mentoring others

Formation

Bachelor's in science/health/business

Master's/MD/PhD in related field

Description du poste

Emory University in Atlanta, GA is seeking a Clinical Research Coordinator II responsible for administrating clinical trial activities, managing study data and assisting with regulatory submissions.

The role requires evaluating participant eligibility, coordinating procedures, and ensuring protocol adherence while mentoring staff and supporting recruitment efforts. Remote work is possible with in-person campus commute as needed.