Role Description
This role will work on the qualitative interviews of study participants with opioid use disorder and chronic pain for the VOICE study, which is evaluating a virtual group therapy intervention and a care management app for individuals receiving buprenorphine treatment in primary care.
Position Responsibilities
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Perform data collection and quality control of study data.
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Develop recruitment methods.
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Oversee the process by which participants are recruited into the study.
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Provide feedback to the study team regarding the interview guide and suggest changes to the interview guide to generate more meaningful data.
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Submit amendments to the IRB as needed, and address IRB stipulations as they arise.
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Review and revise interview transcripts to ensure accuracy.
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Using Dedoose software, assist in the development of codebooks and conduct coding and analysis of textual data for qualitative analysis.
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Input interview transcripts and the codebook into Dedoose.
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Keep a log of all changes made to the codebook throughout the course of the study.
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Collaborate with the Principal Investigators and study team to conduct thematic analysis of the coded data.
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Comply with all HIPAA and Human Subjects Requirements.
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Report urgent issues and adverse events immediately to the Investigators or study staff.
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Ensure confidentiality of study participants is maintained, including with secure storage and transfer of study documents.
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Participate in weekly or biweekly study meetings with investigators and study staff to discuss study requirements and progress, advise about any issues, and receive feedback.
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Communicate with the investigators and study staff in a timely way to ensure effective communication about study-related updates or schedule changes.
Qualifications
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Bachelor's degree required.
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Research and clinical experience are preferred.
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Flexibility and willingness to work evenings and weekends may be needed.