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 role requires strong interpersonal skills, attention to detail, and strict adherence to study protocols, regulatory requirements, and ethical research standards.

This is an on-site, part-time position that pays $20 per hour. You will be expected to work 30 hours per week.

Start date: August 17th, 2026

End date: January 29th, 2027

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

• Serve as a primary point of contact for enrolled subjects, responding to questions related to study participation, visits, and procedures
• Provide ongoing support to promote subject compliance, engagement, and retention throughout the study lifecycle

• Schedule, coordinate, and manage subject study visits in alignment with protocol‑defined timelines and visit windows

• Confirm subject availability and provide visit reminders as needed
• Prepare visit materials and ensure all protocol‑required assessments and procedures are completed accurately and within required windows

• Maintain accurate inventory control, accountability, and reconciliation of investigational products
• Receive, store, dispense, and return IP in accordance with study protocols, sponsor requirements, and regulatory standards.

• Collaborate effectively with monitors, the Clinical Project Management team, and site staff to support overall study success
• Assist in the recruitment and scheduling of site subjects via phone screening of potential participants

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

• Attention to Detail
• Multitasking
• Technical Proficiency
• Flexibility