Jobs at Adams Clinical

Lead site-level clinical operations for inpatient and outpatient studies, managing staff, regulatory compliance, enrollment, safety reporting, budgets, facilities, vendor relationships, and sponsor communications to ensure high-quality trial execution.

The Clinician - Rater conducts clinical interviews, diagnostic evaluations, and assessments for psychiatric and neurological conditions in support of clinical trials, ensuring compliance with standards and collecting reliable data.

The Clinician - Rater conducts clinical interviews and evaluations for psychiatric and neurological trials, ensuring high-quality assessments and compliance with GCP standards.

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.

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.

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

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.

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.

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.

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.