Clinical Advisor

• Provide technical and scientific oversight of the clinical laboratory
• Ensure laboratory quality programs and services meet regulatory standards and established policies and procedures
• Collaborate with laboratory leadership to maintain standardized workflows
• Perform, coordinate, monitor, and report quality assurance actions and issues
• Review quality control, quality assurance, proficiency testing, and equipment service and preventive-maintenance records
• Provide on-site, telephone, or electronic consultation to clinic laboratory personnel
• Prepare clinic laboratories for COLA and CLIA validation surveys and facilitate surveys
• Coordinate inspection information, documentation, and data-gathering procedures
• Identify knowledge gaps and provide in-service education
• Evaluate testing personnel competency and proficiency
• Perform direct-observation competency assessments at required frequencies
• Resolve technical problems and ensure corrective actions for deviations from performance specifications
• Monitor quality indicators and provide timely feedback to staff
• Manage inventory responsibly and support company financial goals
• Represent laboratory services as a subject-matter expert in cross-departmental presentations and projects
• Support new clinical and pathology test offerings, technology enhancements, workflow or system changes, and analyzer/equipment upgrades
• Maintain compliance with state and federal regulatory agencies
• Work at any location as needed to meet company business needs
• Work overtime with sufficient notice
• Perform other assigned duties and projects

Technical Advisor – Clinical Lab

• Provide clinical expertise to internal and external customers
• Critically evaluate literature to develop, maintain, and update clinical criteria
• Participate actively in cross-functional committees, such as the Therapeutic Assessment Committee
• Contribute to the strategic direction of Express Scripts’ core standard clinical products and services criteria development and/or targeting
• Complete complex clinical projects under supervision
• Provide internal and external clinical presentations supporting standard products or complex clinical concepts
• Provide training and education on clinical concepts
• Update clinical areas on industry standards and contribute to the direction of clinical products and services

Clinical Program Advisor – Express Scripts

• Critically evaluate relevant literature to update clinical areas on industry standards
• Contribute to the direction of the company’s clinical products and services
• Provide clinical expertise to internal and external customers
• Develop, maintain, and update clinical criteria
• Participate in cross-functional committees, including the Therapeutic Assessment Committee
• Contribute to strategic direction for ESI’s core standard clinical products and services criteria development and/or targeting
• Complete complex clinical projects under supervision
• Provide internal and external presentations on standard products and complex clinical concepts
• Provide training and education on clinical concepts