PRN Behavioral Health Technician - 7AM-7PM, 7PM-7AM (weekday and weekend shifts available)

Alcanza Clinical Research•DeLand, FL

3d•Onsite

About The Position

The Behavioral Health Technician provides support to study participants enrolled in clinical trials involving mental health, CNS, or behavioral conditions. Working under the supervision of Investigators, Clinical Research Coordinators (CRCs), and site leadership, this role ensures participant safety, supports protocol adherence, and contributes to high-quality data collection in a structured research environment.

Requirements

An associate’s degree in psychology, behavioral health, or related field and 1 year of experience in a healthcare or behavioral health setting, or an equivalent combination of education and experience, is required.
CPR/BLS certification is required.
Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);
Performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc.
Strong organizational skills and attention to detail.
Well-developed written and verbal communication skills.
Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
Must be professional, respectful of others, self-motivated, and have a strong work ethic.
Must possess a high degree of integrity and dependability.
Ability to work under minimal supervision, identify problems and implement solutions.
Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

Nice To Haves

Experience with CNS studies, psychiatric assessments, or behavioral observation tools is highly preferred.
Experience in clinical research and with extended hour or overnight patient stays is a plus.

Responsibilities

Monitor participant safety, behavior, and overall well-being during study visits, including extended or overnight stays (when applicable)
Support execution of study protocols by assisting CRCs with visit flow, assessments, and participant management
Perform and document observational data per protocol requirements (e.g., mood, behavior, sleep patterns, adverse events)
Assist with inventory of belongings, vital signs collection and routine participant check-ins as delegated
Maintain accurate, timely documentation in source notes and systems in alignment with GCP standards
Ensure adherence to protocol requirements, site SOPs, and regulatory guidelines
Assist in managing the clinical environment to ensure safety, organization, and protocol readiness
Participate in de-escalation and crisis response when necessary, following site training and procedures
Collaborate cross-functionally with CRCs, Investigators, and site leadership to maintain efficient study operations
Ensures study related reports and patient results are reviewed by the Research Coordinator and/or investigator in a timely manner.
Assists the site with recruitment, study activities, and administrative needs as needed.
Maintain a positive, results-oriented work environment, build partnerships within the team, and model teamwork.
Maintains strict confidentiality of patients, employees, customers and company information at all times and adheres to HIPAA Guidelines.
Perform all other duties as requested or assigned.