On-Site Research Interviewer - Part-Time Study Support

Sago; Houston (TX); On-site; USD 17,000 - 24,000; Part time

Job summary

Sago is seeking a Research Project Interviewer (RPI) for a part-time, on-site role in Houston. The position involves supporting recruitment, obtaining informed consent, conducting interviews, and ensuring proper study documentation.

You will collaborate with monitors and site staff to drive successful study execution while upholding participant safety and ethical standards. The role requires a high school diploma with preferred college-level education and experience in market or clinical

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-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

Study coordination

Ethical conduct

MS Office

Education

High school diploma

College degree preferred

Tools

Microsoft Office

Job description

Sago is seeking a Research Project Interviewer (RPI) for a part-time, on-site role in Houston. The position involves supporting recruitment, obtaining informed consent, conducting interviews, and ensuring proper study documentation.

You will collaborate with monitors and site staff to drive successful study execution while upholding participant safety and ethical standards. The role requires a high school diploma with preferred college-level education and experience in market or clinical