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Research Project Interviewer - St. Louis - On site

SagoSt. Louis, Missouri🇺🇸United StatesPosted 13 Jul 2026

Why This Role Stands Out

As a Research Project Interviewer with Sago, you'll gain valuable experience in research operations and contribute directly to impactful studies, benefiting from a company culture recognized for happiness and diversity. If you're detail-oriented and enjoy interacting with people, this on-site role offers a unique opportunity to grow within a leading global research partner. Apply today to become part of an exceptional team!

Quick Overview

Salary
$15/hr
Seniority
Mid Senior
Employment type
Part Time
Work mode
On Site
Location
St. Louis, Missouri, United States
Posted
2 months ago
Market ResearchClinical ResearchComplianceMicrosoft Office

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 $15.45 per hour.

Start date: Early August 2026.

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
  • 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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