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Head of Clinical Quality Operations
Company | Talkiatry |
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Location | New York, NY, USA |
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Salary | $175000 – $180000 |
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Type | Full-Time |
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Degrees | |
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Experience Level | Senior, Expert or higher |
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Requirements
- 7-10 years of operational experience within a healthcare setting, with an emphasis on data-driven decision-making and execution.
- Strong project management skills, with the ability to lead complex, cross-functional initiatives.
- Strong ability to recommend creative solutions using data visualization tools, e.g. SQL, Excel, Tableau, Looker, MicroStrategy, Omni, or PowerBI.
- Exceptional presentation and communication skills and the ability to convey the usefulness of insights, reports and analysis to internal and external stakeholders who are not data savvy.
- Familiarity with value-based metrics and their role in quality-driven healthcare models or an interest in learning about them.
- Experience developing clinical pathways and protocols to standardize and improve patient care.
Responsibilities
- Develop a quality roadmap, including metrics, baseline, targets, and dashboard views.
- Collaborate with clinical leadership to roll out internal policies and protocols and launch new internal products.
- Use existing data infrastructure to build out clinical quality dashboards and run ad hoc analyses to develop new metrics.
- Create insights into our clinical quality and safety metrics and develop tangible insights on how we can improve care across the practice.
- Liaise with L&D and Clinical Education to translate findings into proprietary training delivered to clinicians and non-clinicians.
- Manage projects related to the launch and integration of tech and AI solutions, leading to reliable systems of care and quality outcomes.
- Support the Safety Committee to drive accountability across clinical and non-clinical teams.
- Facilitate timely completion of root causes analyses (RCA) where needed for safety events.
- Be embedded as a team of 3 with the National Director of Clinical Quality and Staff Quantitative Scientist to support research initiatives, including IRB submissions.
- Influence clinical leadership through data-backed recommendations and strategic insights, and represent the Quality and Safety function in high-profile meetings and external engagements.
- Have a willingness and ability to become CPHQ certified within a year of starting the role.
Preferred Qualifications
- Research experience including familiarity with IRB submission / publication regulatory requirements.