Part-Time Clinical Research Interviewer

Sago; Woodbridge Township (NJ); On-site; USD 19,000 - 25,000; Part time

Job summary

Sago seeks a part-time, on-site Research Project Interviewer (RPI) in New Jersey to support subject recruitment, informed consent, and study visits. You will work closely with monitors and site staff to ensure proper documentation and protocol adherence.

Qualifications include a high school diploma; college degree preferred or equivalent experience; familiarity with market or clinical research is a plus; strong Microsoft Office skills are beneficial for daily tasks.

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-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

Subject recruitment

Informed consent

Education

High school diploma

Tools

Microsoft Office

Job description

Sago seeks a part-time, on-site Research Project Interviewer (RPI) in New Jersey to support subject recruitment, informed consent, and study visits. You will work closely with monitors and site staff to ensure proper documentation and protocol adherence.

Qualifications include a high school diploma; college degree preferred or equivalent experience; familiarity with market or clinical research is a plus; strong Microsoft Office skills are beneficial for daily tasks.