Clinical Research Coordinator II: Trial Ops & Regulation

Emory University

Atlanta (GA)

On-site

USD 60,000 - 80,000

Full time

3 days ago
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Job summary

Emory University in Atlanta is seeking a Clinical Research Coordinator II to manage administrative activities for clinical trials, maintain databases, develop flow sheets, and ensure source documentation accuracy. The role requires guiding staff and coordinating study tasks within a rigorous regulatory framework.

The position involves determining participant eligibility, consent, recruitment activities, and coordination of supplies.

Qualifications

  • 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.

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.

Skills

Clinical trial management
Regulatory knowledge
Ethics & consent

Education

Bachelor’s degree in health-related field
Master’s degree, MD or PhD
LPN license

Job description

Emory University in Atlanta is seeking a Clinical Research Coordinator II to manage administrative activities for clinical trials, maintain databases, develop flow sheets, and ensure source documentation accuracy. The role requires guiding staff and coordinating study tasks within a rigorous regulatory framework.

The position involves determining participant eligibility, consent, recruitment activities, and coordination of supplies.

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