Research Project Interviewer - Orlando - On site

Research Project Interviewer

• Orlando
• On site Sago
• 3.

2 Orlando, FL Job Details Part-time $15 an hour 22 hours ago Qualifications Computer operation Clinical research Research ethical considerations Computer literacy Filing High school diploma or GED Schedule management Market research Clinical research compliance Patient recruitment Productivity software Entry level Full 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 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 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