Research Assistant I/II - Psychiatry and Behavioral Sciences' REaKT

UTHealth Houston • Houston, TX

3d • Onsite

About The Position

The Research Assistant will support clinical research studies conducted within the inpatient psychiatric services at the UTHealth Houston Center for Interventional Psychiatry, located at the John S. Dunn Behavioral Sciences Center. This role involves direct interaction with participants experiencing major depressive disorder, treatment-resistant depression, and acute suicidal ideation who are enrolled in clinical trials evaluating electroconvulsive therapy (ECT), ketamine, and other interventional psychiatry treatments. Responsibilities include participant screening and recruitment, study assessments, data collection, regulatory documentation, and coordination of study procedures in a fast-paced clinical environment. Given the early scheduling of ECT treatments, work hours begin at 6:00 AM. This role supports clinical research activities by conducting participant recruitment, screening, informed consent, and study visits, while coordinating trials involving ECT, ketamine, and other interventional psychiatry treatments. The Research Assistant will perform comprehensive pre-screening assessments and detailed medical record reviews to determine participant eligibility; collect clinical, cognitive, behavioral, and biological data in accordance with study protocols; ensure participant safety by monitoring and promptly escalating concerns; collaborate closely with psychiatrists, nursing staff, ECT teams, sponsors, and research personnel to uphold protocol compliance; and provide ongoing support for data entry, quality control, and study closeout activities.

Requirements

• Bachelor's degree required.
• May substitute required education with equivalent years of experience beyond the minimum experience requirement.
• None (minimum experience)
• Employees must permanently reside and work in the State of Texas.

Nice To Haves

• Bachelor's degree in Psychology, Neuroscience, Biology, Public Health, Nursing, or a related health science field.
• Prior experience in clinical research, healthcare, mental health, or patient-facing settings preferred.
• Knowledge of Good Clinical Practice (GCP), human subjects’ protection, and research ethics.
• Strong organizational, communication, and interpersonal skills.
• Proficiency with electronic data capture systems (RedCap and Epic).
• Ability to maintain confidentiality and comply with HIPAA requirements.
• Experience working with psychiatric populations, particularly individuals with depression, treatment-resistant depression, or suicidal ideation.
• Experience coordinating clinical research studies and interacting with study participants.
• Familiarity with ECT, ketamine treatments, or other interventional psychiatry procedures.
• Experience with source documentation, regulatory compliance, and electronic case report forms (eCRFs).
• Current Human Subjects Protection and GCP certifications or willingness to obtain certification upon hire.

Responsibilities

• Conduct participant recruitment, screening, informed consent, and study visits.
• Coordinate trials involving ECT, ketamine, and other interventional psychiatry treatments.
• Perform comprehensive pre-screening assessments and detailed medical record reviews to determine participant eligibility.
• Collect clinical, cognitive, behavioral, and biological data in accordance with study protocols.
• Ensure participant safety by monitoring and promptly escalating concerns.
• Collaborate closely with psychiatrists, nursing staff, ECT teams, sponsors, and research personnel to uphold protocol compliance.
• Provide ongoing support for data entry, quality control, and study closeout activities.
• Conduct basic/translational research which may include animal work and other activities according to research protocol.
• Handle biological samples, laboratory experiments and activities, and data collection.
• Collects, organize and prepares research data to provide needed information to principal investigators and other researchers.
• Updates notebooks, records, and databases as needed.
• Maintains clean laboratory equipment and/or work area to ensure a safe and efficient work environment.
• Orders laboratory and/or other supplies as directed by senior research staff.
• Stays abreast of new and updated procedures and protocols for the research laboratory.
• Maintains compliance with required training.
• May participate in continuing education programs, seminars, and workshops.
• May coordinate the work of technicians to ensure efficient, timely and high-quality results.
• Performs other duties as assigned.

Benefits

• 100% paid medical premiums for our full-time employees
• Generous time off (holidays, preventative leave day, both vacation and sick time – all of which equates to around 37-38 days per year)
• The longer you stay, the more vacation you’ll accrue!
• Longevity Pay (Monthly payments after two years of service)
• Awesome retirement/pension plan!
• Free financial and legal counseling
• Free mental health counseling services
• Gym membership discounts and access to wellness programs
• Other employee discounts including entertainment, car rentals, cell phones, etc.
• Resources for child and elder care

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level