About The Position

The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials. Job responsibilities will include data acquisition with a research device in a clinical setting. Participant recruitment/consenting/interaction, database management, IRB protocol compliance and record keeping. Construction of optical sensors, along with assistance on a variety of other miscellaneous experiments in the lab and clinic. The candidate is expected to be self-motivated, detail oriented, have strong interpersonal skills, and capable of working in a collaborative environment.

Requirements

  • High School Diploma or GED and three years of administrative support experience.
  • Two years of college in a scientific, health related, or business administration program and one year of admin support or customer service experience.
  • Licensed as a practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience.
  • Bachelor's degree, Master's degree, MD or PhD in a scientific, health related or business administration program.
  • Clinical training requirements must be tracked and monitored through Emory Healthcare under the credentialing category of Clinical Researcher.

Nice To Haves

  • Self-motivated
  • Detail oriented
  • Strong interpersonal skills
  • Capable of working in a collaborative environment

Responsibilities

  • Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry.
  • Assists with patient recruitment.
  • Attends study meetings.
  • Orders and maintains equipment and supplies.
  • Reviews medical records and/or conducts screenings for recruitment of study participants, performs interviews and QOL questionnaires.
  • Collects study specimen according to protocol which may include phlebotomy, processing, and preparation for shipping.
  • Coordinates services, schedules procedures, creates and maintains case packages, and monitors charges.
  • Assists with quality assurance and tracks regulatory submissions.
  • Performs related approved responsibilities as required.
  • Data acquisition with a research device in a clinical setting.
  • Participant recruitment/consenting/interaction, database management, IRB protocol compliance and record keeping.
  • Construction of optical sensors, along with assistance on a variety of other miscellaneous experiments in the lab and clinic.

Benefits

  • Emory University does not discriminate in admissions, educational programs, or employment, including recruitment, hiring, promotions, transfers, discipline, terminations, wage and salary administration, benefits, and training.

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What This Job Offers

Job Type

Full-time

Career Level

Entry Level

Education Level

High school or GED

Number of Employees

5,001-10,000 employees

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