Find a jobRecruiters

Research Project Interviewer - Houston - On site

Exclusive opportunity

Onsite

Research Project Interviewer - Houston - On site

Sago

Research Project Interviewer - Houston - On site

Skills

ComplianceMarket Research

2 months ago

Share this opportunity

Share this opportunity to other talents of your network:
✓ Offer them a visibility boost with clients.
✓ Help your contacts find their next job.

Important information


Contract type:

Part time

Location:

Houston, TX, USA

Work mode:

Onsite

Published on:

18 August 2026

What they need


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.

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

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

Other offers great for you!

These companies are also looking for great profiles

Wikeys

Project Manager

Freelance

Luxembourg

Hybrid

Skills

AutoCADGestion de projets immobilierssuivi de chantiersTechniques spéciales du bâtimentMarchés publicsMicrosoft OfficeMS ProjectMéthodes AgileCisco

5 hours ago

Quick apply

FreelanceRepublik

Project Manager Saas / ATS (F/H)

Freelance

Paris, France

Hybrid

Skills

SAASMigrationATSCoordination transversaleSanté

5 hours ago

Quick apply

Salutech

Architecte IA - Dijon - Banque

500

Freelance

21000 Dijon, France

Remote, Onsite

Skills

AngularJavaRESTful APIsAIAgile CoachingEnterprise architectureInformation systems urbanizationBanking architecture

4 hours ago

Quick apply

The best place to find your next move

© 2026. All Rights Reserved.

Talents

Find a job

Create a profile

Solutions and tools