Research Project Interviewer - Baltimore - PT

Posted 2 days ago

schlesinger groupBaltimore (MD)

Survey Researchers Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)

SENIORITY

Junior

SALARY

$18.00 per hour

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About the role

Research Project Interviewer 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 $18 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

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