Research Project Interviewer - Baltimore - PT

Sago•Baltimore, MD

2d•Onsite

About The Position

Sago, formerly Schlesinger Group, is a 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. 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.

Requirements

High school diploma required
Strong computer literacy, including proficiency with Microsoft Office applications
Attention to Detail
Multitasking
Technical Proficiency
Flexibility

Nice To Haves

College degree preferred or equivalent relevant work experience
Experience in market research, clinical research, or a related field preferred

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