ABOUT ADAMS CLINICAL

Adams Clinical is a leading clinical trial site network specializing in late-stage neuroscience research. With a strong track record of operational excellence and data quality, Adams Clinical partners with pharmaceutical and biotech sponsors to accelerate the development of life-changing treatments for psychiatric and neurological conditions.

POSITION SUMMARY:

Adams Clinical is seeking entry-level applicants for a Clinical Research Coordinator at our overnight inpatient research facility at our Bronx, NY location. This facility will support cutting-edge clinical trials focused on investigational treatments for acute schizophrenia and other psychiatric conditions.
The Inpatient CRC plays an essential role in the execution of clinical trials within an inpatient research setting, working closely with participants, the Inpatient Unit research team, and study sponsors to ensure adherence to protocols, regulatory compliance, and participant safety. This is a unique opportunity for individuals looking to gain hands-on experience in both clinical research and direct patient care while working in a mission-driven, collaborative environment.

QUALIFICATIONS:

· Bachelor’s degree (required)
· Strong attention to detail, organizational and time-management skills
· Excellent written and verbal communication
· Comfortable engaging with psychiatric populations in a structured inpatient setting
· Willingness to learn hands-on clinical skills such as phlebotomy, ECGs, and vital signs
· Ability to maintain confidentiality and adhere to ethical standards
· Proficient in Microsoft Office Suite
· Prior clinical research experience is a plus, but not required

· Support in the coordination of day-to-day operations at an inpatient psychiatric research unit
· Screen research subjects for participation in industry-sponsored clinical trials involving investigational treatments for schizophrenia, mood disorders, and related psychiatric conditions
· Support study-related inpatient research activities such as admission, study assessments, medication administration tracking, safety monitoring, and discharge
· Collaborate with a cross-disciplinary research team of Principal and Sub-Investigators, Inpatient Unit Manager and Mental Health Technicians to ensure participant safety, well-being, and quality of care throughout their stay
· Perform study procedures (e.g., collecting medical and psychiatric history, vital signs and ECG, phlebotomy, lab specimen processing) according to sponsor-provided protocols
· Maintain accurate source documentation and ensure compliance with Good Clinical Practice (GCP) and regulatory requirements
· Assist with investigational product (IP) accountability, including receipt, storage temperature and inventory monitoring, and documentation in compliance with study protocol and regulatory guidelines
· Communicate regularly with study sponsors regarding trial progress and data collection
· Receive training on inpatient-specific workflows, safety protocols, and de-escalation procedures
· Assist with data entry, query resolution, and audit preparation to ensure inspection readiness