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Schlesinger Group

Research Project Interviewer

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What they do

An Interviewer interviews persons by telephone, mail, in person, or by other means for the purpose of completing forms, applications, or questionnaires. Ask specific questions, record answers, and assist persons with completing form. May sort, classify, and file forms.

$48,345 / year median in Pennsylvania

-25% projected decline

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Job Description

On-siteClinicalPart time Philadelphia, Pennsylvania, United States
OVERVIEW
APPLICATION Share this 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 $17 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 Apply for this job This website uses cookies to improve user's experience, personalise ads and analyse traffic. You can accept all cookies, decline all optional cookies, or manage your cookie settings. To learn more, view our cookies policy. Cookies settings Accept all Decline all Sago collects and processes personal data in accordance with applicable data protection laws. If you are a European Job Applicant see the privacy notice for further details. If you are a California Job Applicant see the privacy notice for further details. Sago does not discriminate on the basis of race, sex, color, religion, age, national origin, marital status, disability, veteran status, genetic information, sexual orientation, gender identity or any other reason prohibited by law in provision of employment opportunities and benefits. View website View all jobs Help Accessibility Cookie settings Powered byWorkable