Per Diem Lead Dosing Session Monitor

Posted 8/24/2026 · last confirmed live 8/26/2026

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 make  the  difference. 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’ll  find:     A culture of respect, transparency, and continuous improvement     Opportunities for professional growth and learning     A team dedicated to improving lives through innovation and integrity     If  you’re  passionate about making an impact  in  clinical research and want to be part of a collaborative, mission-driven organization,  we’d  love to have you on our team.     Job Role   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  P er Diem Lead Dosing Monitor/Therapist for exciting clinical trials focused on psychedelic research for individuals with depression, anxiety, and other mood disorders at one or more   of   our research   site   locations .   Willingness to travel between regional sites is a  plus  but not required. Key Responsibilities   Serve as  Lead  Study Therapist  in psychedelic clinical trials for depression, anxiety, and other mood disorders. Complete  study-sponsored therapist training,  and Adams Clinical site-specific training requirements. Provide support to participants throughout the clinical trial in alignment with the  study protocol and training guidelines. Collaborate with clinicians and site staff managing participant participation in the study. Qualifications   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 ensure  accurate  observation, 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 meet  fixed scheduling expectations , including consistent on-site availability. Final candidate must be approved by both  Adams Clinical and the study sponsor.      Commitments This is a per diem, as-needed position, with work hours based on study enrollment, participant availability, and trial timelines. Therapists should anticipate approximately  2-3 days per week of direct participant-facing responsibilities . These include pre-dose preparation, real-time monitoring during psychedelic dosing sessions, and post-dose follow up sessions. The exact schedule will vary based on  study volume, participant availability, and internal scheduling priorities .  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 include  administrative tasks, onboard, and study-related training , as well as other tasks assigned.   Pay: $125 for training $150 for working Benefits: 401(k) / 401(k) matching Adams Clinical is committed to being an equal opportunity and affirmative action employer. We focus on hiring and nurturing top talent. All employment decisions, including recruitment, hiring, promotion, compensation, transfer, training, discipline, and termination, are made based on the candidate's or employee's qualifications relevant to the position. These decisions are made without regard to age, sex, sexual orientation, gender identity or expression, genetic information, race, color, creed, religion, ethnicity, national origin, citizenship, disability, marital status, military status, pregnancy, or any other legally protected status.   In compliance with federal law, all individuals hired must, as a condition of employment, provide documentation verifying their identity and authorization to work in the United States and complete Form I-9 within the required timeframe. Adams Clinical participates in E-Verify to confirm employment eligibility.  

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