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Clinical Research Coordinator Job Description

Clarigent Health, a Mental Health Technology Company located in Mason, Ohio, is looking for Clinical Research Coordinators to serve as interviewers of research participants for a research study beginning immediately. This study aims to collect data to continue development of a clinical decision support tool that detects and monitors risk for suicide through a participant’s speech.  

Position duties include:

 · Using a virtual platform to conduct a 30-60-minute interview of study participant (time slots are one hour each)

· Complete consent process, interview, and wrap-up 

· Complete all study-related documents (online)

· Communication with the Clarigent team regarding any study protocol deviations, issues, or concerns

Other details:

· Interviewer will participate in study-related training (online)

· Interviewer will sign up for availability each week (no set hours, sign up for what slots you’re available)

· Interviewer will conduct interview and enter interview-related data into online portal

Promote current deals:

· Responsible for coordinating and managing participant study visits

· Conducts study interviews

· Responsible for ensuring study is in compliance with local and federal laws and regulations

·  Screens potential study participants and performs study assessments

· Creates and/or maintains all documents and records related to the study

· Acts as a point of reference for study participants by answering questions and keeping them informed on the study progress

· Manages the inventory of equipment and supplies related to the study 

· Inputs data and patient information into electronic systems

· Creates reports on each study, including notes on protocols, workload, data collection, and more


· Mental Health Counseling/ Social Work/ Psychiatry/ Psychology Graduate student or equivalent (experience on a crisis line or similar warmline or hotline preferred)

· Experience with clinical interviewing 

· Experience as crisis text line or phone line volunteer or suicide prevention programs volunteer is a bonus

· Excellent written and verbal communication skills

· Superior organizational and time management skills

· Capable of working independently with minimal supervision and also as part of a team

· Skilled with standard computer programs including the MS Office suite/ teleconference ie Zoom 

· CITI (human subjects research) training not required but highly desired

Hours: Based on your availability. We would like 3-5 timeslots/interviews per week if possible. These hours can be daytime, evening, or weekends.

Pay: $15.00 an hour

For more information and/or to set up an interview, please contact Human Resources at

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