Teams at IQVIA

Lead end-to-end delivery of real-world observational oncology studies within a pharma FSP, managing cross-functional teams, vendors, study documentation, timelines, budgets, risks, and regulatory compliance while generating reports and driving continuous improvement.

Leads regulatory strategy engagements and real-world evidence programs supporting regulatory decision-making across the product lifecycle. Advises clients on EMA, FDA, MHRA, Health Canada, and PMDA expectations; shapes study designs, submission strategies, and regulatory pathways. Owns delivery quality, client relationships, proposals, business development, and follow-on opportunities. Provides intellectual leadership, mentors junior consultants, builds team capabilities, and contributes to regulatory intelligence and recruitment.

Conducts clinical coding audits, data-quality reviews, benchmarking, and deep-dive analyses for healthcare clients. Produces reports and dashboards, leads SHMI and clinical quality initiatives, facilitates clinician engagement, and provides training on coding, casemix, and data interpretation. Oversees coding services, supports operational quality and productivity, advises clients, develops CCA products, and manages consulting projects and workstreams.