Clinical Research Coordinator II - Rollins School of Public Health

Emory Healthcare • Atlanta, GA

419d • Remote

About The Position

The Clinical Research Coordinator II at Emory University plays a vital role in managing and conducting clinical trials, particularly focusing on environmental health research. This position involves overseeing research project databases, guiding less experienced staff, and ensuring compliance with research protocols. The coordinator will work closely with research participants, manage recruitment strategies, and collaborate with a diverse research team to advance understanding of health impacts related to environmental exposures.

Requirements

• High School Diploma or GED and five years of clinical research experience.
• Or two years of college in a scientific, health related, or business administration program and three years clinical research experience.
• Or a licensed as a practical nurse (LPN) and two years clinical research experience.
• Or a Bachelor's degree in a scientific, health related, or business administration related program and one year of clinical research experience.
• Or a Master's degree, MD or PhD in a scientific, health related or business administration program.

Nice To Haves

• Detail oriented
• Ability to work independently
• Ability to meet deadlines
• Experience using electronic medical records systems
• Bilingual (English and Spanish)
• Strong interpersonal skills
• Enjoys team science and being part of a diverse research team

Responsibilities

• Manages research project databases, develops flow sheets and other study related documents, and completes source documents/case report forms.
• Provides guidance to less experienced staff.
• Interfaces with research participants, determines eligibility and consents study participants according to protocol.
• Approves orders for supplies and equipment maintenance.
• Assists in developing recruitment strategies and conducting screenings for study participants including interviews and questionnaires.
• Supervises collection of study specimens and processing.
• Establishes case packages for study procedures, monitors scheduling of procedures and charges, coordinates other services as needed.
• Ensures compliance with research protocols, reviews case report forms and audits for accuracy with source documents, attends monitoring meetings with sponsors.
• Prepares regulatory submissions.
• With appropriate credentialing and training may perform phlebotomy or diagnostics.
• Performs related approved responsibilities as required.

What This Job Offers

• Job Type: Full-time
• Industry: Ambulatory Health Care Services
• Education Level: High school or GED