Dosing Session Monitor
Adams Clinical
Dosing Session Monitor
Adams Clinical
Performs late-phase, double-blind psychiatric trials
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:
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 Part-Time Psychedelic Dosing Monitor / Therapist 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. Willingness to travel between regional sites is a plus but not required.
Key Responsibilities
Qualifications
Preferred Qualification:
Commitments
Pay: $60.00 - $76.00 per hour
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.
Performs late-phase, double-blind psychiatric trials
Adams Clinical runs late-phase psychiatric and neurologic clinical trials under FDA rules, using double-blind, randomized, placebo-controlled designs to test investigational drugs that have already shown initial promise. Nine full-time doctors act as neutral observers to ensure unbiased results, and coordinators with medical training help maintain data integrity through careful participant selection and standardized procedures. They provide external testing required by law (21 CFR Part 54) for the pharmaceutical industry, earning revenue from pharma companies seeking evidence of efficacy and safety. Their goal is to produce reliable, high-quality data that regulators can use to make decisions on new psychiatric and neurologic drugs, with a special focus on depression research.
Explore more opportunities at Adams Clinical