Psychedelic Dosing Session Monitor

Psychedelic 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 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

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 more of our research site locations. You will be at the forefront of psychedelic research. You'll facilitate preparation, dosing, and integration sessions for participants facing complex mood disorders. You'll also master study-specific protocols, collaborate with a multidisciplinary clinical team and maintain rigorous ICH-GCP standards to ensure data integrity and participant safety.

Key Responsibilities:

• Serve as StudyTherapist in onsite 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.

What Success Looks Like

• You successfully balance intensive on-site clinical sessions with efficient remote follow-ups, ensuring participant safety and protocol adherence.
• You are fully onboarded and proficient in study-specific training, proactively handling administrative and clinical responsibilities to keep the trial running smoothly.

Salary: $125 - $200 per hour

Benefits:

• 401(k) matching
• Employee assistance program
• Paid time off

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.