Jobs at Adams Clinical

The Lead Dosing Session Monitor will act as the primary therapist during psychedelic clinical trials, providing support to participants and collaborating with clinicians.

Assist in psychedelic dosing sessions for clinical trials, ensuring participant safety and adherence to study protocols under supervision. Collaborate with clinical teams and fulfill administrative tasks as needed.

Support psychedelic clinical trials as an Assistant Dosing Session Monitor, ensuring protocol adherence and participant safety under supervision, while collaborating with a clinical team.

The Assistant Psychedelic Dosing Session Monitor supports psychedelic clinical trials, ensuring participant safety and protocol adherence while collaborating with clinicians and site staff.

Provide entry-level support for site-based clinical trials: participant scheduling and liaison, screening assistance, vitals/ECGs/specimen collection (as trained), data entry into EDC, source document management, supply and IP support, and preparation for monitoring and audits under CRC supervision, following GCP and site SOPs.

Oversee site-level clinical operations at the Watertown facility, leading staff and study teams to ensure enrollment, protocol adherence, safety/SAE reporting, regulatory compliance, ALCOA documentation, vendor and facilities oversight, budget monitoring, and sponsor communications to deliver high-quality trial execution.

The Clinical Research Coordinator II manages complex clinical trials, ensuring study execution, participant visits, communication with sponsors, and data quality oversight.

Manage budgets, contract administration, and sales operations for clinical trials. Collaborate with teams to ensure contract compliance and drive process improvements.

The Office Coordinator supports daily site operations, manages participant scheduling, communication, and maintains office environment while ensuring positive participant experiences.

Support participant evaluation, triage, and enrollment for clinical trials: prep materials, assist prescreening, collect vitals/labs, maintain source documents, enter data into EDC, coordinate visits, and support consent and participant flow under clinician supervision.

Own end-to-end payroll for a multi-site, multi-state clinical organization using Rippling. Process semi-monthly and off-cycle payroll, maintain records, reconcile reports in Excel, respond to employee inquiries, support benefits and year-end tax processes, and maintain audit-ready compliance documentation.

The Clinical Research Coordinator III manages complex clinical trials, ensures data integrity and enrollment targets, and supervises research staff. They lead study operations, support site performance metrics, and train junior staff while acting as the main contact for sponsors and monitors.

The Assistant Psychedelic Dosing Session Monitor supports clinical trials for mood disorders, ensuring participant safety and protocol adherence while collaborating with a clinical team.

The Inside Sales and Marketing Specialist will identify clinical trial opportunities, support marketing initiatives, maintain a pipeline in Salesforce, and assist with administrative duties within the business development team.

The Clinical Research Assistant supports clinical trials by assisting with participant interactions, data management, regulatory compliance, and operational tasks under supervision.

As a Principal Investigator, the psychiatrist will oversee study protocols, ensure participant safety and regulatory compliance, and guide clinical trial processes at the site.

Adams Clinical seeks a Psychiatrist to serve as Principal Investigator, ensuring participant safety and conducting evaluations in clinical trials. Responsibilities include collaborating with clinical operations, performing assessments, managing participant eligibility, and maintaining compliance with regulatory standards.

Manage and optimize full-funnel digital advertising across multiple self-serve platforms, analyze performance and cohorts, create and test ad creative and landing pages, support website and listings improvements, coordinate sponsor/IRB creative approvals, and recommend new digital trends to grow recruitment and conversions.

Provide administrative and regulatory support for clinical trials: prepare and maintain study documents and regulatory files, assist with IRB submissions and renewals, track staff training/certifications, and help ensure records are audit-ready and compliant with applicable regulations.

Support participant evaluation, triage, and enrollment for clinical trials. Prepare study materials, assist prescreening and informed consent, collect demographics and basic clinical data, perform vitals and lab collections (training provided), maintain source documentation, and enter data into EDC systems to ensure compliant, efficient study operations.