On-Site Part-Time Research Interviewer: Consent & Visits

Sago; St. Louis (MO); On-site; USD 21,000 - 23,000; Part time

Job summary

Sago, the global research and data partner, is seeking a part-time, on-site Research Project Interviewer (RPI) to support recruitment, informed consent, study visits, and documentation. The role starts in August 2026 and pays $15.45 per hour in St.

Louis, MO. Responsibilities include conducting interviews, explaining study objectives, obtaining informed consent, coordinating visits, and partnering with monitors and site staff to ensure protocol adherence and subject safety.

Qualifications

• High school diploma required.
• College degree preferred or equivalent 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-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

Communication

Education

High school diploma

College degree preferred or equivalent experience

Tools

Microsoft Office

Job description

Sago, the global research and data partner, is seeking a part-time, on-site Research Project Interviewer (RPI) to support recruitment, informed consent, study visits, and documentation. The role starts in August 2026 and pays $15.45 per hour in St.

Louis, MO. Responsibilities include conducting interviews, explaining study objectives, obtaining informed consent, coordinating visits, and partnering with monitors and site staff to ensure protocol adherence and subject safety.