• Lead the development of integrated global medical plans that drive asset strategy and scientific excellence in lupus • Provide strong medical and scientific input to shape clinical, evidence generation, and launch readiness activities • Interpret and communicate complex clinical data to both internal and external stakeholders with scientific precision and clarity • Contribute to data generation efforts, including registrational, post-approval, and investigator-initiated studies • Partner with cross-functional teams (Clinical Development, Regulatory, HEOR, Commercial, and others) to ensure alignment and scientific integrity • Build and maintain trusted relationships with key external experts, professional societies, and advocacy groups • Provide clinical leadership during congress planning, advisory boards, and educational activities • Collaborate effectively across functions and with external partners to ensure scientific consistency and alignment across medical deliverables

• Provide study, project and program-specific medical monitoring and review services • Leading of all medical aspects of contracted tasks • Supervising of safety variables • Discussing with clients, investigators and healthcare professionals of medical issues in the pre and post approval services by using accurate medical judgment, interpretation and decision • Provide medical consultation to team members and answer study related medical questions • Communicate clearly with associates and clients, maintaining an open line of communication to ensure all procedures are followed appropriately • Analysis and assessment of safety data to identify and run emerging safety signals • Medical review of individual case safety reports, serious adverse event reports and clinical outcome reports. • Assist in Business Development activities • Present PPD standard medical safety processes to clients at business development meetings and connect with various medical communities to explore and expand PPD business • Participate in training of project teams • Provide therapeutic and protocol training as needed • Write, review and approve reports, regulatory submissions and protocols, ensuring that the medical content is accurate and complete.

• Provide medical oversight, expertise and leadership to ensure the delivery of cost effective, quality healthcare services to health plan members • Serves as clinical advisor to and educator of medical management staff making sure correct clinical judgment is applied to all medical management determinations • Provide leadership and expertise in the development, implementation and interpretation of medical review and quality related policies and guidelines • Provide oversight and direction for staff and provider training and education • Promote positive relations with the local medical community, including periodic consultation with providers or prescribers • Review case management data, identifies trends and gaps in care and recommends corrective actions • Review all quality of care issues and oversees the development and implementation of processes for improvement • Monitor performance indicators to ensure the delivery of cost-effective care within quality standards • Monitor member and provider satisfaction and recommends and implements changes to improve satisfaction levels • Work collaboratively to develop corporate clinical care standards and medical practice policies • Provide medical guidance to the Medical Management department

• Lead the design and implementation of clinical development programs • Oversee education of investigators and study personnel • Lead clinical study teams and monitor overall study integrity • Present at scientific and regulatory meetings globally • Develop relationships with academic investigators • Author clinical sections for regulatory filings • Maintain knowledge of compliance and regulatory requirements • Participate in business development activities as required