Clinical Research Coordinator II: Trials & Team Support

Emory University

Atlanta (GA)

On-site

USD 55,000 - 75,000

Full time

14 days+

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Job summary

Emory University in Atlanta is seeking a Clinical Research Coordinator II to manage administrative activities for clinical trials. You will maintain project databases, develop flow sheets and case report forms, and ensure accurate data capture and regulatory compliance.

You will coordinate participant screening, informed consent, and scheduling, while supporting junior staff and liaising with sponsors. This role requires multitasking, attention to detail, and adherence to protocol.

Qualifications

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

Responsibilities

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

Skills

Clinical research
Data management
Regulatory docs

Education

High School diploma or GED + 5 years clinical research
Associate degree in a scientific/health related or business program + 3 years clinical research
LPN license + 2 years clinical research
Bachelor's degree in science/health/business + 1 year clinical research
Master's/MD/PhD in science/health/business

Job description

Emory University in Atlanta is seeking a Clinical Research Coordinator II to manage administrative activities for clinical trials. You will maintain project databases, develop flow sheets and case report forms, and ensure accurate data capture and regulatory compliance.

You will coordinate participant screening, informed consent, and scheduling, while supporting junior staff and liaising with sponsors. This role requires multitasking, attention to detail, and adherence to protocol.

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