Lead Dosing Session Monitor

Join Us in Shaping the Future of Clinical Research

Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. Our mission is simple: deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare. Our vision is to set the gold standard for clinical trial excellence. We believe our people makethedifference. Guided by our core values—Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration—we create an environment where meaningful work drives meaningful change.

At Adams Clinical,you’llfind:

• A culture of respect, transparency, and continuous improvement
• Opportunities for professional growth and learning
• A team dedicated to improving lives through innovation and integrity

Ifyou’repassionate about making an impactinclinical research and want to be part of a collaborative, mission-driven organization,we’dlove to have you on our team.

Adams Clinical is a rapidly growing research site network specializing focused on late phase industry-sponsored trials of novel treatments for a variety of psychiatric and neurological conditions.

We are seeking a
per diem Psychedelic Dosing Monitor/Therapist
for exciting clinical trials focused on psychedelic research for individuals with depression, anxiety, and other mood disorders at one or moreofour researchsitelocations.

Willingness to travel between regional sites is aplusbut not required(Watertown and Boston; Harlem and Bronx).

• Serve asLeadStudy Therapist in psychedelic clinical trials for depression, anxiety, and other mood disorders.
• Complete study-sponsored therapist training,and Adams Clinical site-specifictrainingrequirements.
• Provide support to participants throughout the clinical trial in alignment with thestudy protocol and training guidelines.
• Collaborate with clinicians and site staff managing participant participation in the study.

• Licensed mental health professional in Massachusetts, New York, Pennsylvania, or Texas(e.g., PsyD, PhD, LCSW, LMSW, LMHC, LMFT), with the ability to provide psychotherapy in compliance with state regulations
• Attention to detail is critical for this role to ensureaccurateobservation, documentation, and reporting of dosing sessions, with strict adherence to ICH-GCP standards and protocol requirements.
• Experience working with individuals with depression, anxiety, or other mood disorders
• Strong interpersonal and communication skills, with an interest in advancing mental health care in a clinical research setting.
• Ability to meetfixed scheduling expectations, including consistent on-site availability.
• Final candidate must be approved by both Adams Clinical and the study sponsor.

• Thisisaperdiem,as-neededposition,withworkhoursbasedonstudyenrollment, participant availability, and trial timelines.
• Therapists should anticipate approximately2-3daysperweekofdirectparticipant-facing responsibilities.
  
  Theseincludepre-dosepreparation,real-timemonitoringduringpsychedelicdosingsessions,andpost-dosefollowupsessions.
  
  Theexactschedulewillvarybasedonstudyvolume,participantavailability,andinternalschedulingpriorities.
• Flexibility and responsiveness to shifting scheduling needs are essential.
• A majority of the participant appointments must be conducted in person at our research site locations, and a portion can be conducted remotely by the therapist
• Therapists must be willing to learn and adhere to ICH-GCP standards.
• Additional responsibilities includeadministrative tasks, onboard, and study-related training, as well as other tasks assigned.

$60.00 - $70.00 per hour

• 401(k) / 401(k) matching

Adams Clinical is committed to being an equal opportunity and…