About The Position

The Clinical Research Coordinator II handles administrative activities generally associated with the conduct of clinical trials. This position will support an NIH National Institute on Aging (NIA)-funded R01 study, "Improving Residual Sleepiness and Inflammation in Older Adults with OSA: A Randomized Controlled Trial of Citicoline," led by Principal Investigator Dr. Victoria Pak in collaboration with a multidisciplinary team of investigators, including Co-Investigator Dr. Lynn Marie Trotti, Director of the Emory Sleep Center. The coordinator will oversee the day-to-day operations of the study, including participant recruitment, study visits, data collection, biospecimen processing, and regulatory activities.

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

  • Experience with REDCap, participant recruitment, regulatory documentation, and coordination of clinical trials is strongly preferred.
  • Phlebotomy certification and experience performing venipuncture and processing biospecimens are strongly preferred.

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.

Benefits

  • Emory University offers a comprehensive benefits package including health, dental, and vision insurance.
  • Retirement savings plan.
  • Paid time off.
  • Professional development opportunities.
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