Psychedelic Facilitator

Job Summary

Segal Trials’ Center of Psychedelic and Cannabis Research at Segal Trials is honored to be the gold standard private research site in the US. An integral role in the clinical trial involving a psychedelic is that of a facilitator. As a facilitator for Segal Trials, you will be a licensed mental health professional or have a BA in psychology or related field with at least one year of experience in a licensed mental health clinical setting. They service clients by providing a safe, judgment-free environment with supportive conversation, empathetic resilience, and flexible direction.

The Facilitator is responsible for the dosing session monitoring and facilitation of psychedelic research clinical trials testing new treatments on behalf of the sponsor/pharmaceutical companies. This individual promotes Good Clinical Practices (GCP) in the conduct of Clinical Investigations by ensuring the integrity of data generated at the site and directing the conduct of the clinical investigation as to the guidelines issued by State and Federal Authorities and the Sponsor. The Facilitator works collaboratively with the study team and regulatory personnel to ensure welfare of study participant and oversees execution of the study protocol, delegates study related duties to site staff, as appropriate, and ensures site compliance with study protocols, study specific laboratory procedures, and standards of Good Clinical Practice.

DUTIES & ESSENTIAL JOB FUNCTIONS

• Adhere to the established SOPs and WIs when performing delegated tasks.
• Facilitate preparatory, dosing post-dosing, and psychoeducation sessions as required by the protocol.
• Respond to Subjects’ concerns/calls in a timely manner.
• Attend Pre-Study Site Visits and Site Initiation Visits as necessary.
• Attend Study-specific meetings as necessary.
• Review and follow study-specific facilitator & dosing session manuals.
• Complete study-specific facilitator training as required by the sponsor/CRO and any contracted entities conducting such training
• Maintain ongoing study-specific training requirements as required by the sponsor/CRO and any contracted entities conducting such training
• Regularly check and respond to work emails regarding ongoing facilitator duties and study-specific tasks, including protocol training and other requirements.
• Maintain all required licenses and credentials to practice and execute the job as Facilitator
• Disclose conflicts of interest as described in the regulations.

Work Location: In person