Why This Role Stands Out
This on-site Research Project Interviewer role offers a fantastic opportunity to contribute to impactful research by directly engaging with participants and ensuring study integrity. You'll thrive here if you have strong communication and organizational skills, and enjoy a role that fosters meticulous attention to detail within a highly-rated company culture. Apply today to become a key part of Sago's mission to connect human answers to business questions.
Quick Overview
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 $18 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
- 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
Similar jobs
- CS
Biospecimen Coordinator I
Cynet Systems
Tucson, AZ🇺🇸Hybrid2 months agoComplianceMicrosoft ExcelMicrosoft Word+2 - SG
Microbiology Intern (8 Month Contract)
NewSGS
Fairfield, NJ🇺🇸On-site8 hours ago - EU
Analyst II, Eurofins Environment Testing South Central, Stafford, TX
NewEurofins
Stafford, TX🇺🇸$25 - $30/hrOn-site2 days agoCompliance - PA
PhD Research Intern - Robotics & Physical AI
NewPalona AI
Los Altos, California🇺🇸On-siteYesterdayMachine LearningRoboticsComputer Vision+5 - TA
Senior R&D Technician, Space PV Prototyping
NewTandempv
Fremont🇺🇸On-site2 days agoAssembly - EX
Research Associate
Expa
Remote US🇺🇸Remote3 days agoHugging FaceLESS