Jobs at Adams Clinical

Serve as Lead Study Therapist in psychedelic clinical trials: complete study and site training, provide pre-dose preparation, real-time monitoring and post-dose follow-up, document observations per ICH-GCP and protocol, collaborate with clinicians and site staff, and maintain on-site availability for participant-facing sessions (majority in person).

Provide entry-level support for clinical trial site operations including participant scheduling and liaison, basic screening, vitals/ECG/specimen collection (as trained), source documentation, EDC data entry, supply and IP support, and maintenance of study records to ensure regulatory and protocol compliance under CRC supervision.

Manage complex, high-enrolling clinical trials including screening, enrollment, visits, data entry, IP accountability, regulatory readiness, sponsor liaison, supervising junior staff, and presenting study metrics.

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.

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.

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.

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 foundational support for site-level clinical trials: assist with study start-up, participant screening and scheduling, perform vital signs/ECGs/specimen collection as trained, complete ALCOA+-compliant source documentation, enter data into EDC, maintain study binders/logs, support monitoring visits, assist with IP accountability, and follow site SOPs and GCP under direct supervision.

Entry-level Clinical Research Assistant supporting site-level clinical trial operations. Duties include participant scheduling and liaison, basic vitals/ECGs/specimen collection as trained, data entry into EDC, source documentation (ALCOA+), study supply and binder maintenance, support for monitoring visits, IP accountability assistance, and learning site SOPs and GCP compliance.

Provide operational and participant-facing support for clinical trials including scheduling, screening, specimen collection, vital signs and ECGs (as trained), data entry into EDC, source documentation per ALCOA+, supply and binder management, support monitoring visits, and assist with IP accountability under direct supervision.

Provide fast, friendly Tier I IT support (in-person and remote) for a 350-person clinical research operation. Triage and document incidents, assist with VoIP, Windows/Mac troubleshooting, Microsoft 365 administration, hardware procurement, asset management, and contribute to internal documentation.

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.

Provide lead therapist coverage for industry-sponsored psychedelic clinical trials: complete study training, deliver psychotherapy before/during/after dosing, collaborate with clinical team, follow protocol and ICH-GCP, perform administrative tasks, and maintain consistent on-site availability (three days/week).

Support onsite psychedelic dosing sessions under a Lead Monitor’s supervision, ensuring participant safety and protocol adherence. Complete study and site training, collaborate with clinical staff, observe and document dosing sessions per ICH-GCP, perform administrative onboarding tasks, and maintain consistent on-site availability (three days/week). May travel between regional sites as needed.

Support onsite psychedelic dosing sessions under the Lead Dosing Session Monitor, ensuring participant safety, protocol and ICH-GCP adherence, accurate observation and documentation, and collaboration with clinicians. Complete study and site training, perform administrative tasks, and maintain consistent on-site availability for scheduled dosing days to support trial operations.