Part-Time On-Site Research Interviewer

卡杯; Iselin (PA); On-site; USD 18,000 - 26,000; Part time

Job summary

Sago is seeking a part-time on-site Research Project Interviewer (RPI) to support recruitment, consent, visits, and study documentation. The role includes interacting with subjects, explaining study details, and ensuring proper documentation and compliance.

Responsibilities include scheduling visits, collaborating with monitors and project management, and maintaining ethical conduct focused on participant safety.

Qualifications

• 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.

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

Skills

Interviewing

Informed consent

Study coordination

Microsoft Office

Education

High school diploma

College degree preferred

Tools

Microsoft Office

Job description

Sago is seeking a part-time on-site Research Project Interviewer (RPI) to support recruitment, consent, visits, and study documentation. The role includes interacting with subjects, explaining study details, and ensuring proper documentation and compliance.

Responsibilities include scheduling visits, collaborating with monitors and project management, and maintaining ethical conduct focused on participant safety.