• Research Project Interviewer - Part Time

    Schlesinger Group (St. Louis, MO)


    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

    We are seeking a dedicated and detail-oriented individual to join our research team as a Research Interviewer for a short-term protocol-driven study. This individual will play a key role in Subject-facing study activities and assist with protocol-specific tasks in coordination with the Study Nurse and Sponsor Monitor.

     

    This is a part-time position making $15 per hour.

    Job Description

    + Obtain informed consent from Study Subject in accordance with GCP and protocol guidelines.

    + Conduct Subject intake visits, including completion of baseline surveys and study questionnaires.

    + Assist during the device patch application process (performed by the Study Nurse) by photographing the application site in accordance with protocol procedures.

    + Coordinate with the Nurse and Study Team to ensure smooth participant flow during visits.

    + Conduct interim follow-up phone calls to monitor Subject well-being and assess for any adverse events (AEs) or protocol deviations.

    + Maintain accurate call logs and report any safety concerns promptly to the Study Team.

    + Assist during the final Subject visit where the device patch is removed by the Study Nurse.

    + Support final survey collection and ensure Subjects are compensated appropriately.

    + Maintain Good Clinical Practice (GCP) certification; must either have valid certification or be willing to complete certification prior to study start (training provided if needed).

    Requirements

    + Excellent interpersonal and communication skills; comfortable working directly with Subjects.

    + Strong attention to detail, organizational skills, and ability to follow detailed study protocols.

    + Ability to maintain confidentiality and ensure data integrity.

    + GCP certification (required before study start; training can be provided).

    + Basic proficiency with electronic data capture and ability to manage photo documentation.