On-Site Part-Time Research Interviewer

Sago; Philadelphia (Philadelphia County); On-site; USD 19,000 - 28,000; Part time

Job summary

Sago is seeking a part-time, on-site Research Project Interviewer in Philadelphia to support subject recruitment, consent, and study visits. The role involves handling investigational product documentation and coordinating visits, with a focus on participant safety and protocol adherence.

Ideal candidates have a high school diploma (college degree preferred) and experience in market or clinical research, plus strong Microsoft Office skills for data entry and reporting.

Qualifications

• High school diploma is required.
• College degree or equivalent work experience is preferred.
• Experience in market research, clinical research, or related field is preferred.
• Strong computer literacy, including Microsoft Office applications.

Responsibilities

• Conduct subject interviews to assess preliminary eligibility in accordance with study protocols and 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 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 participant-focused research.

Skills

MS Office proficiency

Education

High school diploma

College degree or equivalent work experience

Tools

Microsoft Office

Job description

Sago is seeking a part-time, on-site Research Project Interviewer in Philadelphia to support subject recruitment, consent, and study visits. The role involves handling investigational product documentation and coordinating visits, with a focus on participant safety and protocol adherence.

Ideal candidates have a high school diploma (college degree preferred) and experience in market or clinical research, plus strong Microsoft Office skills for data entry and reporting.