Senior Clinical Trial Research Interviewer (ETS) | Temporary
About The Position
The Senior Clinical Trial Research Interviewer recruits, screens, identifies, contacts, and interviews participants for assigned research projects. Interviews are conducted by telephone. The role coordinates data collection, schedules appointments, obtains consent, explains studies to participants, and collects data. It may involve abstracting information from medical records, observing participants and recording observations in writing or by video, and designing forms, worksheets, and study questionnaires. The interviewer edits questionnaires, follows up to resolve missing or unclear data, may code and enter information into a database, and compiles data and reports for research analysis. The position also provides direction to others involved in interviewing and maintains required records. The role requires a high school diploma or equivalent, two years of administrative support, customer service, or related experience including one year of interviewing experience, and data-entry experience. A position requiring blood draws also requires completion of a phlebotomy training program. The role is temporary. It offers regular work from home, with the ability to commute to an Emory University location as needed. Biweekly employees must reside in Georgia. Emory may change the work-from-home status with notice.
Requirements
- High school diploma or equivalent.
- Two years of administrative support, customer service, or other related experience, including one year of interviewing experience.
- Data-entry experience.
- For positions requiring blood draws, completion of a phlebotomy training program.
- Must be able to commute to an Emory University location as needed.
- Biweekly employees must reside within the State of Georgia.
Responsibilities
- Recruit, screen, identify, contact, and interview participants for assigned research projects.
- Conduct interviews by telephone.
- Coordinate the data collection process.
- Abstract data from participants’ medical records when needed.
- Schedule appointments, obtain consent forms, explain studies to participants, and collect data.
- Observe participants and document observations in writing or by video when needed.
- Edit completed questionnaires for completeness, legibility, and accuracy.
- Follow up with participants to obtain missing data or clarify existing data.
- Design forms, worksheets, and study questionnaires.
- Code and enter data into a database when needed.
- Compile data and produce reports for analysis of research findings.
- Provide direction to others engaged in the interviewing process.
- Maintain required records.
- Perform related responsibilities as required.
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What This Job Offers
Career Level
Senior
Education Level
High school or GED
