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How much do multidisciplinary association for psychedelic studies jobs pay per hour?

As of Jun 17, 2026, the average hourly pay for multidisciplinary association for psychedelic studies in the United States is $85.94, according to ZipRecruiter salary data. Most workers in this role earn between $67.07 and $93.99 per hour, depending on experience, location, and employer.

Where is psychedelic research being done?

Psychedelic research is conducted at various academic institutions, nonprofit organizations, and specialized research centers worldwide. These institutions often focus on studying therapeutic uses of psychedelics, requiring researchers to have backgrounds in psychology, neuroscience, or pharmacology, and sometimes involve clinical trials regulated by health authorities.

What is the Multidisciplinary Association for Psychedelic Studies (MAPS)?

The Multidisciplinary Association for Psychedelic Studies (MAPS) is a nonprofit research and educational organization dedicated to developing medical, legal, and cultural contexts for people to benefit from the careful uses of psychedelics and marijuana. Founded in 1986, MAPS funds clinical research, public education, and advocacy related to the therapeutic use of substances such as MDMA, psilocybin, and cannabis. Its work focuses on supporting scientific studies, raising awareness about psychedelic-assisted therapies, and advancing policy reform. MAPS has been instrumental in progressing clinical trials for MDMA-assisted therapy for post-traumatic stress disorder (PTSD).

What types of roles and collaborative projects might I expect when working at the Multidisciplinary Association for Psychedelic Studies (MAPS)?

Working at MAPS often involves cross-functional collaboration between researchers, clinicians, policy experts, and community outreach teams. You may participate in clinical research trials, educational initiatives, or advocacy campaigns, depending on your role. The environment is typically mission-driven and dynamic, with team members working closely to advance psychedelic research and public education. Collaboration across disciplines is key, and professionals are encouraged to bring innovative ideas to complex projects while navigating regulatory and ethical considerations.

What is the Multidisciplinary Association for Psychedelic Studies?

The Multidisciplinary Association for Psychedelic Studies (MAPS) is a nonprofit organization that conducts research on the therapeutic potential of psychedelics and related substances. It employs scientists, researchers, and clinicians to advance scientific understanding and develop medical treatments involving psychedelics within regulated environments.

What are the key skills and qualifications needed to thrive as a psychedelic research associate, and why are they important?

To thrive as a psychedelic research associate, you need a solid background in psychology, pharmacology, or neuroscience, often evidenced by an advanced degree and research experience. Familiarity with clinical trial protocols, data analysis software (such as SPSS or R), and regulatory compliance (e.g., IRB processes) is typically required. Strong interpersonal skills, attention to detail, and ethical sensitivity help in working with vulnerable populations and multidisciplinary teams. These skills ensure rigorous, ethical research and contribute to the advancement of safe, evidence-based psychedelic therapies.

What does maps stand for psychedelics?

In the context of the Multidisciplinary Association for Psychedelic Studies, MAPS stands for the Multidisciplinary Association for Psychedelic Studies, a nonprofit organization dedicated to research and education on the medical and therapeutic uses of psychedelics. Job roles within MAPS may involve research, clinical trials, and policy advocacy related to psychedelic substances.

How can I become part of psychedelic research?

To join psychedelic research, individuals typically need a background in fields such as psychology, neuroscience, or pharmacology, along with research experience and relevant certifications. Positions may include research assistant, coordinator, or scientist, often requiring familiarity with clinical trial protocols and ethical standards. Gaining experience through academic programs, internships, or volunteering at research institutions can improve chances of involvement.
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Multidisciplinary Association For Psychedelic Studies jobs near you
Infographic showing various Multidisciplinary Association For Psychedelic Studies job openings in the United States as of June 2026, with employment types broken down into 86% Full Time, and 14% Part Time. Highlights an 86% In-person, and 14% Hybrid job distribution, with an average salary of $178,751 per year, or $85.9 per hour.
Assistant Psychedelic Dosing Session Monitor

Assistant Psychedelic Dosing Session Monitor

Adams Clinical

Watertown, MA • On-site

$50 - $60/hr

Per diem

Retirement, PTO

Posted 9 days ago

Job description

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 Assistant Psychedelic Dosing Monitor to support clinical trials focused on psychedelic research for individuals with depression, anxiety, and other mood disorders at one or more of our research site locations. In this role, you will support dosing sessions under the supervision of the Lead Dosing Session Monitor, ensuring participant safety and protocol adherence throughout the trial. You'll collaborate with a multidisciplinary clinical team, complete study-specific training, and uphold rigorous ICH-GCP standards to support data integrity and participant wellbeing. Willingness to travel between regional sites is a plus, but not required (e.g., Watertown and Boston; Harlem and Bronx).
Key Responsibilities:
  • Serve as Assistant Dosing Session Monitor in onsite psychedelic clinical trials for depression, anxiety, and other mood disorders.
  • Complete study-sponsored 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.
  • Fulfill additional responsibilities including administrative tasks, onboarding, and study-related training as assigned.

What Success Looks Like
  • You maintain consistent, dependable on-site availability three days per week (Monday-Wednesday or Tuesday-Thursday), supporting participant-facing dosing sessions under the Lead Dosing Session Monitor's supervision.
  • You are fully onboarded in study-specific protocols and ICH-GCP standards, contributing to smooth trial operations through accurate observation, documentation, and reporting.

Qualifications:
  • Minimum of 1 year of experience in a mental healthcare setting including clinical research experience as a Clinical Research Coordinator or in a comparable role supporting psychiatric research studies
  • Bachelors degree from accredited institution; Clinical sciences, Psychology or Nursing focus is a plus
  • 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

Preferred:
  • Prior experience with industry-sponsored psychedelic clinical trials (e.g., Compass, Cybin, MindMed, Atai)

Job Location: On-site work located at Watertown, MA; Boston, MA; Harlem, NY; Bronx, NY; Philadelphia, PA; or Dallas, TX.
Job Type: Per Diem (PRN)
Expected hours: Approximately 24 hours per week (flexible based on site needs and prn employee availability)
Compensation: $40 per training hour; $50-60 per hour working 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.

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