Director Clinical Quality

Anovorx Group LLCMemphis, TN

About The Position

The Director, Clinical Quality is responsible for leading accreditation and clinical quality initiatives within the Quality department, with a primary focus on accreditation readiness, audit preparedness, process improvement, CAPA support, and clinical quality metrics. This role serves as a Quality department resource supporting accreditation management, process improvement, audit readiness, CAPAs, and quality oversight activities across the organization. The position partners cross-functionally with operational and support departments to help ensure accreditation standards, quality expectations, and regulatory or contractual requirements are effectively incorporated into workflows, documentation, monitoring activities, and quality initiatives.

Requirements

  • Bachelor’s degree in Pharmacy, PharmD, preferred.
  • Active Pharmacist license in good standing
  • Minimum 10 years of pharmacy or healthcare experience
  • Minimum 5 years of accreditation, quality, audit, or compliance-related experience
  • Experience leading accreditation readiness, accreditation surveys, and ongoing accreditation management, including direct ownership of accreditation activities rather than support-only involvement
  • Experience with URAC, ACHC or similar accreditation standards
  • Experience with CAPA management, process improvement initiatives, and quality oversight activities
  • Experience developing, monitoring, and reporting quality metrics and accreditation-related KPIs
  • Experience interpreting accreditation standards and translating requirements into operational workflows, policies, and documentation
  • Experience participating in and leading audits, inspections, or accreditation surveys
  • Experience supporting implementation or oversight of operational or clinical workflow updates
  • Experience supporting organizational growth initiatives, launches, or expansion activities
  • Strong understanding of accreditation standards, quality systems, and audit readiness expectations
  • Ability to interpret standards and translate requirements into operational workflows and quality activities
  • Strong analytical and problem-solving skills
  • Ability to lead cross-functional discussions and drive follow-up actions
  • Strong organizational and project management skills
  • Ability to manage multiple priorities and deadlines simultaneously
  • Strong written and verbal communication skills
  • Ability to work independently and collaboratively across departments
  • Ability to identify process improvement opportunities and support implementation of corrective actions and quality initiatives

Nice To Haves

  • PharmD

Responsibilities

  • Lead and support accreditation readiness activities for URAC, ACHC, and other applicable accreditation standards.
  • Coordinate accreditation evidence preparation, standards interpretation, gap assessments, and ongoing readiness activities.
  • Partner with the Director, Quality Operations to support inspection and audit readiness initiatives.
  • Support development, implementation, and monitoring of accreditation-related metrics and quality KPIs.
  • Lead or support process improvement initiatives related to patient management, operational workflows, and accreditation findings.
  • Collaborate cross-functionally to identify process gaps, compliance risks, and quality improvement opportunities.
  • Support CAPA investigations, corrective actions, effectiveness monitoring, and process improvement activities related to accreditation or quality findings.
  • Participate in therapy, program, or operational launches to ensure accreditation and quality requirements are incorporated into workflows and documentation.
  • Assist with development, review, and revision of policies, SOPs, work instructions, forms, and quality documentation related to accreditation and quality oversight activities.
  • Participate in Quality Committee, Clinical Oversight Committee, and other cross-functional meetings as needed.
  • Support implementation and quality oversight of clinical software updates, assessments, protocols, and documentation workflows.
  • Serve as a resource for interpretation of accreditation standards and quality expectations impacting operational workflows.
  • Support preparation and presentation of accreditation and quality metrics for leadership meetings, committees, and audits.
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