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Research Project Interviewer - Orlando - On site
Sago —Orlando, FL
- $15 an hour
- Part-time
- Computer literacy
- High school diploma or GED
- Experience equivalent to degree accepted
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Research Project Interviewer - Orlando - On site

Sago -
Orlando, FL

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Job Details

Part-time
$15 an hour

Qualifications

Computer operation
High school diploma or GED
Desktop applications
Productivity software

Full Job Description

Sago, formerly Schlesinger Group, is the global research and data partner that connects human answers to business questions. Combining our legacy of impact, global reach, and innovative spirit, we enable our clients to solve business problems through extensive audience access and an adaptive range of qualitative and quantitative solutions. We help our clients understand what their customers want and demand — empowering them to make decisions with confidence. As a partner to our clients, their clients, and the industry, Sago seamlessly connects businesses to key insights.

Join our team at SAGO, where happiness thrives in the top 35%, our work culture ranks in the top 10%, and diversity shines in the top 15% compared to peers of our size. Discover more about us at https://www.comparably.com/companies/sago

Position Summary

The Research Project Interviewer (RPI) plays a critical role in the successful execution of research studies by supporting subject recruitment, informed consent, study visits, investigational product handling, and study documentation.

This is a part-time and on-site position making $15 per hour.

Key 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

Requirements

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

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