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Manager Psychedelic information

What are the key skills and qualifications needed to thrive as a Manager in the Psychedelic sector, and why are they important?

To thrive as a Manager in the Psychedelic sector, you need a solid background in clinical research, mental health, or life sciences, often supported by relevant degrees and leadership experience. Familiarity with regulatory frameworks, clinical trial management systems, and compliance certifications such as GCP (Good Clinical Practice) is typically required. Outstanding communication, ethical judgment, and team leadership skills set top candidates apart in this field. These skills ensure the safe, effective, and compliant advancement of psychedelic therapies in a rapidly evolving and highly regulated landscape.

What does a Manager Psychedelic do?

A Manager Psychedelic oversees the operations and administration of programs or clinics that use psychedelic substances for therapeutic or research purposes. They are responsible for ensuring compliance with legal regulations, coordinating staff such as therapists and medical professionals, and managing patient care protocols. Additionally, they may handle outreach, education, and collaboration with researchers or partners. Their role is crucial in maintaining safety, ethical standards, and efficiency within psychedelic-assisted therapy settings.

What are some common challenges faced by a Manager in the Psychedelic sector and how are they typically addressed?

Managers in the Psychedelic sector often encounter challenges related to navigating complex regulatory environments, ensuring ethical compliance in clinical trials, and maintaining open communication between interdisciplinary teams. Staying current with evolving laws and best practices is crucial, as is fostering a culture of safety and transparency when working with sensitive substances. Successful managers prioritize ongoing professional development and collaborate closely with legal, clinical, and research professionals to address these challenges effectively.
More about Manager Psychedelic jobs
What cities are hiring for Manager Psychedelic jobs? Cities with the most Manager Psychedelic job openings:
What are the most commonly searched types of Psychedelic jobs? The most popular types of Psychedelic jobs are:
What states have the most Manager Psychedelic jobs? States with the most job openings for Manager Psychedelic jobs include:
Infographic showing various Manager Psychedelic job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution.
Assistant Psychedelic Dosing Session Monitor

Assistant Psychedelic Dosing Session Monitor

Adams Clinical

New York, NY โ€ข On-site

$60 - $70/hr

Other

Retirement

Posted 11 hours ago


Job description

Join Us in Shaping the Future of Clinical Researchย 

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 makeย theย 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.ย 

At Adams Clinical,ย you'llย find:ย 

  • A culture of respect, transparency, and continuous improvementย 
  • Opportunities for professional growth and learningย 
  • A team dedicated to improving lives through innovation and integrityย 

Ifย you'reย passionate about making an impactย inย clinical research and want to be part of a collaborative, mission-driven organization,ย we'dย love to have you on our team.ย 

Job Roleย 

We are seeking a per diem (PRN) 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).ย 

Key Responsibilities:ย 

  • Serve as Assistant Dosing Sessionย Monitor inย onsite psychedelic clinical trials for depression, anxiety, and other mood disorders.ย 
  • Complete study-sponsored training and Adams Clinical site-specific training requirements.ย 
  • Provide support to participants throughout the clinical trial in alignment with the study protocol and training guidelines.ย 
  • Collaborate with clinicians and site staff managing participant participation in the study.ย 
  • Fulfillย additionalย responsibilities including administrative tasks, onboarding, and study-related training as assigned.ย 

What Success Looks Likeย 

  • Youย maintainย 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.ย 
  • You are fully onboarded in study-specific protocols and ICH-GCP standards, contributing to smooth trial operations throughย accurateย observation, documentation, and reporting.ย 

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 (exible based on site needs and per diem [PRN] employee availability)

Compensation:ย ย $30 - $40 per training hour; $60-70 per hour working hour

ย Benefits:

  • ย 401(k)
  • ย 401(k) matchingย 
  • ย Per diem employees accrue paid sick leave at a rate of one hour for every 30 hours worked. Accrual caps and pay eligibility are based on total company headcount in accordance with New York State law. This role is based in New York City. Additional leave protections apply under the NYC Earned Safe and Sick Time Act."

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.ย 

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 requiredย timeframe. Adams Clinicalย participatesย in E-Verify to confirm employment eligibility.ย