Onsite Part-Time Research Interviewer

Sago; Atlanta (GA); In loco; USD 18.000 - 26.000; Part-time

Descrizione del lavoro

Sago is seeking a Research Project Interviewer to support study recruitment, consent, and scheduling of subject visits. This part-time, on-site role involves handling informed consent and coordinating visits in line with study protocols.

The position requires a high school diploma, with a college degree preferred or equivalent experience; market or clinical research experience and strong MS Office skills are valued. On-site at the Atlanta area location, starting October 2026.

Competenze

• 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

Mansioni

• 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

Conoscenze

Interviewing

Consent process

Communication

Formazione

High school diploma

College degree preferred or equivalent

Strumenti

Microsoft Office

Descrizione del lavoro

Sago is seeking a Research Project Interviewer to support study recruitment, consent, and scheduling of subject visits. This part-time, on-site role involves handling informed consent and coordinating visits in line with study protocols.

The position requires a high school diploma, with a college degree preferred or equivalent experience; market or clinical research experience and strong MS Office skills are valued. On-site at the Atlanta area location, starting October 2026.