Nurse/Clinical Research Coord
University of New Mexico
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- Location
- Albuquerque, United States
- Job type
- Full time
- Posted
- Oct 13
- 7 days ago
Career path
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About the company
University of New Mexico
Higher education · 2 to 10 employees
What you'll do
- Facilitate psychedelic-assisted therapy sessions in accordance with research protocols, including preparation, medication administration, and integration.
- Document study visits and clinical findings, follow up with participants, and participate in study meetings.
What you need
- Complete required University of New Mexico trainings.
Key skills
FacilitationParticipant careClinical researchSuicidal or homicidal risk
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Read the full posting here
The Department of Family and Community Medicine seeks to hire a 0.25 Nurse/Clinical Research Coordinator. This position will provide professional services and participant care for the UNM Research Program in Psychedelic Assisted Therapies. The individual will be a lead facilitator for the Group Assisted Psilocybin Assisted Therapy (GPAT) for PTSD. There is the potential to be involved with additional psychedelic assisted therapy studies including the MATPOD study using MDMA for postpartum women with Opioid Use Disorder.
GPAT is an innovative study of group Psilocybin Assisted Therapy using an affinity group model including veteran/first responders, women survivors of sexual trauma, and other groups. The model has been created in alignment with a community engagement process. There is the potential for the Nurse/Clinical Research Coordinator to participate in the development of the psychotherapeutic model which will be in context of an FDA approved clinical trial protocol.
Duties and Responsibilities
1. Conduct facilitation in accordance with approved research protocols. Working closely with the study MD and other study staff to implement the facilitation aspects of protocol including preparatory sessions, medication administration sessions, and integration sessions. Ensure that facilitation provided adheres to the research protocol.
2. Conduct full day psychedelictherapy medication sessions lasting about 8 hours and often occurring on weekends.
3. Documentation of study visits, researchquestionnairesand therapy sessions inREDCapand study folders.
4. Follow-upphone calls and emails to study participants.
5. Completion of required checklists/progress notes and other source documents.
6. Evaluating study participants for suicidal or homicidal risk and documenting clinical findings and decisions. Identity patients requiring therapeutic support.
7. Adherence to required completion deadlines for required University of New Mexico trainings and offered on learning central
8. Participate in study group meetings and conference calls.