> Markdown version of [/jobs/ext/4258704-data-coordinator-2](https://www.wearedevelopers.com/jobs/ext/4258704-data-coordinator-2). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Data Coordinator 2 - **Company:** Augusta University - **Location:** Augusta, GA, United States - **Experience:** Experienced - **Salary:** $39,208.0 - **Contract:** Permanent contract - **Skills:** Software Applications, Databases, Internet Security, Microsoft Office - **Published:** October 31, 2026 - **Apply:** https://www.careerbuilder.com/job-details/data-coordinator-2-augusta-ga--ecaf981d-ecf4-471a-b8b6-aeeac11dbbbd ## About the Role Organizational Skills, Healthcare, Internet Security, Healthcare Providers, Medicine, Health Science, Training/Teaching, Patient Care, Public Health, Government, Associates degree from an accredited college or university in a related field. OR Completion of two years of college level coursework and two years of related work experience. Preferred Qualifications Oncology research specific knowledge and experience preferred. Familiarity with medical terminology. Experience in database management software preferably OnCore. Knowledge, Skills, & Abilities Ability to maintain confidentiality High attention to detail and change management Excellent interpersonal, written and verbal communication skills Proficient in Microsoft Office and other computer software/databases Detail-oriented with strong prioritization, multi-tasking, organizational, problem-solving and time-management skills ## Description This position performs a variety of complex duties involved in providing regulatory support for the investigator-initiated trials program in the GCC CTO. Duties include but are not limited to: assist with investigator-initiated IRB submissions including personnel amendments, continuation reports and annual reports (completion of IRB forms and other regulatory forms as needed for each submission), ensuring the submissions are in compliance within federal, stage, and local regulations; assist with submissions to the FDA (annual reports) and completion of FDA forms. Additionally, this position will assist in the preparation of the SIV. Responsibilities The duties include, but are not limited to: IRB Submission support IRB submission support includes the local IRB; completion of all IRB and submission forms, obtaining signatures, completion of training, delegation of duties logs, and all forms pertinent to each submission, etc. Meeting Facilitator Meeting Facilitator support includes assisting in the preparation and facilitation of SIV meetings. FDA Submissions support FDA submissions support includes assisting in the submission of annual reports to the FDA including completion of FDA forms. Software and Data Coordination Software access & data coordination Provide access for study team members in OnCore; track and update study status, task lists. Other Perform all other additional duties as assigned.