Part-Time On-Site Research Interviewer

Sago; Atlanta (GA); On-site; USD 18,184 - 25,898; Part time

Job summary

Sago seeks a part-time on-site Research Project Interviewer in Atlanta to support subject recruitment, informed consent, and study visits. You will help ensure study timelines are met and documentation is accurate.

Responsibilities include conducting interviews to assess eligibility, explaining objectives and risks clearly, obtaining consent, scheduling visits, and collaborating with monitors and site staff to support study success while upholding subject safety and regulatory compliance.

Qualifications

• High school diploma required.
• College degree or equivalent experience preferred.
• Experience in market research, clinical research, or a related field preferred.
• Proficient with Microsoft Office applications.

Responsibilities

• Conduct subject interviews to assess preliminary eligibility in accordance with study protocols and defined inclusion/exclusion criteria.
• Clearly explain study objectives, procedures, risks, and participant responsibilities in a professional and participant-friendly manner.
• Obtain informed consent from eligible subjects prior to initiation of any study-related procedures.
• Ensure informed consent documentation is complete, accurate, and properly filed in compliance with regulatory and sponsor requirements.
• Schedule, coordinate, and manage subject study visits in alignment with protocol-defined timelines and visit windows.
• Collaborate effectively with monitors, the Clinical Project Management team, and site staff to support overall study success.
• Maintain professional, ethical conduct with a strong commitment to subject safety and a participant-focused research approach.

Skills

Interviewing

Informed consent

Communication

Education

High school diploma

College degree preferred

Tools

Microsoft Office

Job description

Sago seeks a part-time on-site Research Project Interviewer in Atlanta to support subject recruitment, informed consent, and study visits. You will help ensure study timelines are met and documentation is accurate.

Responsibilities include conducting interviews to assess eligibility, explaining objectives and risks clearly, obtaining consent, scheduling visits, and collaborating with monitors and site staff to support study success while upholding subject safety and regulatory compliance.