Clinical Risk and Complex Case Research Specialist
ICBD Holdings
full-time
Posted on:
Location: 🇺🇸 United States
Visit company websiteJob Level
Mid-LevelSenior
About the role
- Conduct and synthesize structured case reviews, focusing on risk categories such as behavioral emergencies, trauma, medical comorbidities, and psychiatric complexity.
- Collaborate with the Director of Research to refine and implement research-driven risk frameworks (e.g., Safe-T, structured records reviews).
- Support the translation of risk findings into clinical protocols, staff training, and family support tools.
- Analyze and summarize case-level data to inform clinical decision-making and organizational risk policy.
- Participate in interdisciplinary meetings, offering research-informed recommendations for complex client needs.
- Contribute to scholarly outputs (manuscripts, conference presentations, internal reports) related to clinical risk and safety practices.
- Provide consultation and mentorship to clinical teams on integrating evidence-based risk practices.
- Maintain project records, confidentiality standards, and documentation aligned with IRB and research ethics requirements.
Requirements
- Master’s or Doctoral degree in Behavior Analysis, Education, Psychology, or related discipline
- Active BCBA certification in good standing preferred; other licensure (psychology, counseling, or social work) strongly considered for risk mitigation expertise.
- 5+ years of professional experience supporting individuals with autism and/or complex behavioral and medical needs.
- Demonstrated experience in clinical risk assessment, crisis planning, or safety-focused research.
- Strong collaboration skills with interdisciplinary teams.
- Strong organizational skills and ability to manage multiple priorities across projects and timelines.
- Excellent written and verbal communication skills, including ability to communicate findings to both clinical and non-clinical audiences.
- Comfortable working independently while maintaining collaboration with cross-functional teams and external partners.
- Willingness to travel occasionally to support research activities or represent the organization at professional conferences.
- Successful completion of background check, drug screening, and maintenance of a clean driving record.
- Willingness to sign and comply with the company’s non-disclosure agreement (NDA), including future amendments.
- Co-authorship on peer-reviewed publications or professional conference presentations (preferred)
- Experience coordinating or managing research partnerships with academic or medical institutions (preferred)
- Familiarity with IRB processes, data privacy standards, and applied research ethics (preferred)
- Proficiency with data analysis tools, visualization platforms, or behavior analytic software (e.g., SPSS, Excel, Catalyst, or similar) (preferred)