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Northside Hospital Inc.

Research Associate

Pay: Not specified

Posted: 2 weeks ago

Location: Atlanta, GA (Onsite)

Last Updated: 2 days ago

Hours: Full-Time

Expires: 10/15/2026

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What they do

A Clinical Research Associate is responsible for running clinical trials, usually for an organization undertaking pharmacological drug testing. Will ensure that trials adhere to good clinical practice guidelines for monitoring clinical trials.

$109,276 / year median in Georgia

+2% projected growth

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Job Description

Overview Northside Hospital is award-winning, state-of-the-art, and continually growing. Constantly expanding the quality and reach of our care to our patients and communities creates even more opportunity for the best healthcare professionals in Atlanta and beyond. Discover all the possibilities of a career at Northside today. Responsibilities The Research Associate role supports activities that are integral to the conduct of clinical research at Northside Hospital. Specifically, this position helps support research operations through the execution of departmental projects, leveraging data from and generating reports out of research systems and through supporting clinical research to ensure good clinical practice and protocol compliance. This role routinely works with sensitive or confidential information, documents and issues. Qualifications Bachelor's degree in Biology, Life Science, Health Science, or Public Health. One (1) year of healthcare experience.

PREFERRED

Masters of Science Degree from an accredited college or university in a data driven research-related field (allied health, biological sciences, chemistry, economics, informatics, mathematics, psychology, sociology, epidemiology, public health, etc). Three (3) to (5) years relevant work experience in a Clinical Research setting. Knowledge of key research regulations (e.g., FDA / OHRP / ORI / DHHS / NIH). General understanding of human subject protection and Institutional Review Board regulation and operation. Proficient in applications such as Microsoft Word, Excel, and PowerPoint.

Experience with the following applications:

Onsemble OnCore, Florence eBinders, Florence eConsent, YUNU, CTSU OPEN, Medidata, WCG ClinSphere, IRBNet. Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) through Association of Clinical Research Professional (ACRP) and/or the Society of Clinical Research Associates (SOCRA). Advanced knowledge and understanding of clinical research practices including federal regulations, federal grant and clinical trials policy and regulations, management systems, and technology solutions used to coordinate clinical research. Current and valid certificates of completion for all three (3) of the following Collaborative Institutional Training Initiative (CITI) Program courses relevant to coordination of clinical research.

Work Hours:

7AM-4:30