[Hiring] Quality and Safety Coordinator @Visante Consulting LLC

Role Description

The Quality and Safety Coordinator leads and independently contributes to the organization’s clinical quality and safety initiatives across field services clients under the direction of the Director of Quality and Clinical Programs. This role is responsible for delivering operational, analytical, and coordination support for quality management, safety, and regulatory/accreditation programs.

• Develops, implements, and evaluates metric frameworks.
• Independently oversees data collection and monitoring activities.
• Prepares and interprets analytical reports, providing actionable insights and recommendations to support leadership decision making.
• Analyzes trends and identifies risks and opportunities to contribute to quality performance and continuous improvement efforts.
• Leads the coordination and evaluation of activities related to quality-related events, medication errors, near-miss trends, adverse events, and infection prevention indicators.
• Independently analyzes and interprets data trends, determines appropriate follow-up actions, and monitors effectiveness of improvement initiatives.
• Supports regulatory and accreditation readiness by leading components of policy management processes.
• Partners strategically with internal stakeholders, client quality teams, and clinical pharmacy departments.
• Oversees and facilitates the event escalation processes related to complex patient cases or high-impact clinical or quality events.
• Leads components of clinical competency and standardization initiatives.

Qualifications

• BS or PharmD from an accredited college of pharmacy.
• Master’s degree preferred (e.g., MBA, MHA, MS in Organizational Leadership, or related discipline).

Requirements

• 3+ years of progressive experience in specialty and/or infusion pharmacy, including quality program oversight and interdisciplinary collaboration.
• 1+ years of leadership experience supporting quality program activities and/or accreditation activities.
• Demonstrated experience leading or supporting accreditation readiness, quality management, event review/RCA, and policy governance.
• Demonstrated expertise with sterile compounding quality systems and USP 797/800 practices (preferred).
• Experience partnering with client quality departments and multi-entity clinical pharmacy leadership (preferred).
• Active, unrestricted pharmacist license (RPh) in at least one state; ability to obtain additional licensure as needed.

Benefits

• Competitive salary and benefits for this part-time salaried role.

Equal Opportunity Statement

Visante is an equal opportunity employer. Visante’s people are its greatest asset and provide the resources that have made the company what it is today. Visante is, therefore, committed to maintaining an environment free of discrimination, harassment, and violence.