Research Associate

Northside Hospital; Atlanta (GA); On-site; USD 52,000 - 70,000; Full time

Job summary

Northside Hospital seeks a Research Associate to support clinical research operations by extracting data from research systems and generating reports to ensure protocol compliance and good clinical practice. The role involves handling sensitive information and coordinating with teams on study activities.

The ideal candidate will have a biology or health science background, healthcare experience, and familiarity with research regulations and IRB processes.

Qualifications

• Bachelor's degree in Biology, Life Science, Health Science, or Public Health.
• One year of healthcare experience.
• Masters in a data driven research-related field preferred.
• Three to five years in clinical research preferred.
• Knowledge of key research regulations (FDA / OHRP / ORI / DHHS / NIH).
• Understanding of human subject protection and IRB regulations.

Responsibilities

• Support research operations through data extraction from research systems and generation of reports.
• Assist with research compliance and good clinical practice.
• Handle confidential information and research documentation with care.

Education

Bachelor's degree in Biology / Life Science / Health Science / Public Health

Master's of Science in a data-driven research-related field

Tools

Onsemble OnCore

Florence eBinders

Florence eConsent

YUNU

CTSU OPEN

Medidata

WCG ClinSphere

IRBNet

Job description

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.

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.

1. Bachelor's degree in Biology, Life Science, Health Science, or Public Health.
2. One (1) year of healthcare experience.

PREFERRED:

1. 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).
2. Three (3) to (5) years relevant work experience in a Clinical Research setting.
3. Knowledge of key research regulations (e.g., FDA / OHRP / ORI / DHHS / NIH).
4. General understanding of human subject protection and Institutional Review Board regulation and operation.
5. Proficient in applications such as Microsoft Word, Excel, and PowerPoint.
6. Experience with the following applications: Onsemble OnCore, Florence eBinders, Florence eConsent, YUNU, CTSU OPEN, Medidata, WCG ClinSphere, IRBNet.
7. 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).
8. 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.
9. 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.