Director Clinical Systems Engineering
Indexed description
Day in the Life of a Director Clinical Systems Engineering
Key Responsibilities:
- Lead structured requirements elicitation with clinical, pharmacy, front office, revenue cycle, quality, and compliance stakeholders; facilitate workshops, workflow walkthroughs, and design sessions.
- Translate operational and clinical needs into clearly written functional and technical specifications that can be built, tested, and audited.
- Produce and maintain requirements artifacts, including current- and future-state workflow maps, user stories with acceptance criteria, configuration workbooks, requirements traceability matrices, and test scripts.
- Drive formal requirements review and sign-off prior to build; manage scope, change requests, and downstream impact analysis.
- Evaluate whether business needs are best met through configuration, integration, third-party solution, or process change, and present recommendations with cost, risk, and effort trade-offs.
- Oversee interfaces and data exchange across the application portfolio, including HL7 v2 and FHIR messaging, laboratory and toxicology results, e-prescribing and EPCS, PDMP, pharmacy and dispensing systems, and downstream reporting and analytics feeds.
- Support eligibility, claims, and remittance transaction flows (270/271, 837, 835) through the organization’s clearinghouse and payer channels in partnership with the revenue cycle team.
- Monitor interface queues and error handling; lead root-cause analysis and remediation with vendors, trading partners, and internal IT.
- Develop and validate reports and data extracts using SQL and native reporting tools; ensure data definitions are consistent across systems.
- Independently write, optimize, and troubleshoot complex SQL across clinical, pharmacy, and financial data; build and maintain operational, regulatory, and executive reporting, extracts, and dashboards.
- Own data validation for migrations and system changes, including reconciliation queries, record and field-level validation, exception reporting, and documented sign-off criteria.
- Maintain the enterprise data dictionary and source-to-target mapping; investigate data integrity issues to root cause across configuration, interfaces, and workflow.
- Present findings, methodology, and limitations clearly to clinical, operational, and executive audiences; apply minimum-necessary and 42 CFR Part 2 principles to all reporting and data sharing.
- Serve as the technical lead for site migrations onto the target EHR platform, including data extract and mapping, conversion testing, load validation, cutover planning, go-live support, and post go-live stabilization.
- Define and execute validation protocols for high-risk clinical and financial data, including dosing history, active orders, allergies, diagnoses, consents, and patient balances.
- Coordinate build, testing, and training readiness activities with implementation, help desk, and operations leadership to support wave-based go-lives.
- Document and escalate migration risks, defects, and decisions; maintain issue logs through resolution.
- Directly supervise two Clinical Applications Analysts, including work assignment, prioritization, performance management, coaching, and professional development.
- Establish and enforce intake, triage, and service level standards for application requests; balance project workload against production support escalations.
- Develop team competency in configuration, testing discipline, and documentation; build cross-coverage to reduce single-threaded dependencies.
- Partner with the help desk and implementation teams to ensure clean handoffs between project delivery and ongoing support.
- Manage day-to-day technical relationships with application vendors; review release notes, coordinate upgrades, plan regression testing, and hold vendors accountable to defect resolution timelines.
- Ensure system configuration and documentation support HIPAA, 42 CFR Part 2, DEA, SAMHSA and state OTP requirements, state licensure, CARF or other accreditation standards, and payer requirements.
- Maintain audit-ready records of configuration changes, access reviews, validation testing, and system decisions.
- Report project status, risks, decisions, and key performance metrics to the Vice President, Clinical Applications and to senior leadership.
- Perform other duties as assigned.
- Advanced working knowledge of electronic health record and practice management system architecture, configuration, and release management.
- Demonstrated proficiency in requirements elicitation and documentation methods, including workflow mapping, user stories, functional specifications, and traceability.
- Working knowledge of healthcare integration standards and technologies, including HL7 v2, FHIR, APIs, and secure file transfer.
- Advanced, hands-on SQL proficiency required — including multi-table joins, subqueries, common table expressions, aggregation, and window functions — with the ability to independently query, validate, and reconcile data across disparate systems without analyst support.
- Working knowledge of healthcare EDI transactions and clearinghouse operations.
- Understanding of behavioral health and substance use disorder clinical workflows, documentation, and billing requirements.
- Demonstrated project management skills, including planning, resourcing, risk management, and structured status reporting to executive stakeholders.
- Proven ability to lead, develop, and hold accountable a small technical team.
- Demonstrated data fluency: able to structure an analytical question, validate the underlying data, and present the result credibly to executives. Experience with business intelligence tools and with native EHR report writers.
- Bachelor’s degree in health informatics, information systems, computer science, healthcare administration, or a related field required; Master’s degree preferred. Equivalent combination of education and directly relevant experience will be considered.
- Minimum of seven (7) years of progressive experience in clinical application configuration, systems analysis, or EHR implementation required.
- Minimum of two (2) years of direct people leadership or formal project leadership experience required.
- Demonstrated ownership of end-to-end requirements gathering for clinical or enterprise software initiatives required.
- Hands-on configuration experience with at least one enterprise EHR or practice management platform required; behavioral health, substance use disorder, or OTP platform experience strongly preferred.
- Experience supporting multi-site EHR implementation, consolidation, or data migration required.
- Working knowledge of interfaces and integration (HL7, FHIR, API, SFTP) required. Demonstrated hands-on SQL experience is required and will be assessed during the interview process.
- Knowledge of OTP and OBOT operations, including methadone and buprenorphine dispensing workflows, take-home regulations, and 42 CFR Part 2, strongly preferred.
- Experience with a healthcare clearinghouse and familiarity with revenue cycle workflows preferred.
- Professional certification such as CPHIMS, CAHIMS, PMP, Certified Scrum Product Owner, Six Sigma, or vendor-specific application certification preferred.
- Ability to travel to clinic sites as required to support implementations, go-lives, and workflow assessments.
- Experience building reports, extracts, or dashboards used by operational or executive leadership required; experience owning data validation for a system conversion strongly preferred.
- Medical, Dental, and Vision Insurance
- PTO
- Variety of 401K options including a match program with no vesture period
- Annual Continuing Education Allowance (in related field)
- Life Insurance
- Short/Long Term Disability
- Paid maternity/paternity leave
- Mental Health Day
- Calm subscription for all employees
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