Research Associate

Northside Hospital Inc.; Atlanta (GA); On-site; USD 60,000 - 85,000; Full time

Benefits offered by this job

Health benefits

Job summary

Northside Hospital Inc. is seeking a Research Associate to support clinical research operations, leverage data from research systems, and generate reports to ensure protocol compliance and good clinical practice.

Ideal candidates have a bachelor’s degree in relevant sciences and at least 1 year of healthcare experience, with preferred advanced credentials and experience in various research applications and regulatory guidelines. This on-site role in Atlanta supports ongoing clinical studies.

Qualifications

• Bachelor’s degree in biology, life sciences, health sciences, or public health is required.
• At least 1 year of healthcare experience is required.

Responsibilities

• Support clinical research operations by executing departmental projects and generating reports from research systems.
• Ensure good clinical practice and protocol compliance in research activities.

Skills

Healthcare experience

Education

Bachelor’s degree in Biology, Life Science, Health Science, or Public Health.

Job description

Overview

Northside Hospital is award-winning, state-of-the-arc?? 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-4:30PM

Weekend Requirements:

No