Casual Role-Study Coordinator

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

• Perform data collection and quality control of study data
• Develop recruitment methods
• Oversee the process by which participants are recruited into the study
• Provide feedback to the study team regarding the interview guide and suggest changes to the interview guide to generate more meaningful data.
• Submit amendments to the IRB as needed, and address IRB stipulations as they arise.
• Review and revise interview transcripts to ensure accuracy.
• Using Dedoose software, assist in the development of codebooks and conduct coding and analysis of textual data for qualitative analysis.
• Input interview transcripts and the codebook into Dedoose.
• Keep a log of all changes made to the codebook throughout the course of the study.
• Collaborate with the Principal Investigators and study team to conduct thematic analysis of the coded data.
• Comply with all HIPAA and Human Subjects Requirements.
• Report urgent issues and adverse events immediately to the Investigators or study staff.
• Ensure confidentiality of study participants is maintained, including with secure storage and transfer of study documents.
• 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.
• Communicate with the investigators and study staff in a timely way to ensure effective communication about study-related updates or schedule changes.

Bachelor's degree required. Research and clinical experience are preferred. Flexibility and willingness to work evenings and weekends may be needed.