Research Project Interviewer - Phoenix - PT

卡杯; Phoenix (AZ); On-site; USD 22,730 - 32,373; Part time

Job summary

Sago, a global research and data partner, is hiring a Research Project Interviewer to support recruitment, informed consent, study visits, IP handling, and documentation on-site in Phoenix, AZ.

This part-time role offers $20 per hour and a 30-hour work week, starting August 17, 2026, with end date January 29, 2027. The position requires attention to detail, strong interpersonal skills, and strict adherence to study protocols.

Qualifications

• High school diploma required; college degree preferred or equivalent experience.
• Experience in market or clinical research is advantageous.
• Strong computer literacy and proficiency with Microsoft Office applications.

Responsibilities

• Conduct subject interviews to assess preliminary eligibility according to study protocols.
• Explain study objectives, procedures, risks, and participant responsibilities clearly.
• Obtain informed consent from eligible subjects before procedures.
• Serve as primary contact for enrolled subjects and answer participation questions.
• Support subject engagement and retention throughout the study.
• Schedule and manage subject study visits per protocol timelines.
• Prepare visit materials and ensure all assessments are completed on time.
• Maintain inventory control and reconcile investigational products.
• Receive, store, dispense, and return IP per protocol and sponsor requirements.
• Collaborate with monitors, the Clinical Project Management team, and site staff.
• Assist in recruitment and scheduling via phone screening.

Skills

Attention to Detail

Multitasking

Technical Proficiency

Flexibility

Education

High School Diploma

College degree preferred

Tools

Microsoft Office

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 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

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

Key Skills

• Attention to Detail
• Multitasking
• Technical Proficiency
• Flexibility