Impactful Part-Time Research Interviewer

Sago; Atlanta (GA); On-site; USD 18,000 - 26,000; Part time

Job summary

Sago, a global research and data partner, seeks a part-time Research Project Interviewer at our Atlanta site to support subject recruitment and study logistics.

You will conduct interviews, obtain informed consent, schedule visits, and ensure accurate study documentation while collaborating with monitors and site staff.

A high school diploma is required; a college degree or relevant experience is preferred, and proficiency with Microsoft Office is expected.

Qualifications

• High school diploma required; college degree preferred or equivalent relevant work experience.
• Experience in market research, clinical research, or a related field preferred.
• Strong computer literacy, including proficiency 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

Market research

Clinical research

Microsoft Office

Education

High school diploma

College degree or equivalent

Job description

Sago, a global research and data partner, seeks a part-time Research Project Interviewer at our Atlanta site to support subject recruitment and study logistics.

You will conduct interviews, obtain informed consent, schedule visits, and ensure accurate study documentation while collaborating with monitors and site staff.

A high school diploma is required; a college degree or relevant experience is preferred, and proficiency with Microsoft Office is expected.