Jobs at IQVIA

Lead the Data, Technology, and Advisory Services growth in JAPAC, driving strategy, client engagement, and team development across multiple sectors.

Provide administrative support to CRAs and Regulatory/Start-Up teams to maintain Trial Master File and clinical documentation, track CRFs and supplies, assist with file reviews, communications, and may support on-site monitoring after required training.

Lead and support bespoke qualitative and mixed-method healthcare research: design studies, moderate interviews and focus groups, analyse qualitative and quantitative findings, manage projects and stakeholders, translate evidence and RWE into strategic insights, and deliver presentations and client-facing recommendations.

Provide senior subject-matter expertise in clinical feasibility and enrollment strategy. Lead complex feasibility analyses, synthesize multiple data sources, present recommendations to stakeholders, facilitate cross-functional meetings, train and mentor junior staff, and improve planning processes and tools to support proposals and awarded studies.

Serve as a client-facing SaaS implementation and support expert for a clinical eSource platform. Lead client onboarding, deliver training, troubleshoot technical issues, manage support tickets within SLAs, gather configuration requirements, and collaborate with Engineering, Product, Sales, and Project teams. Support audits, demos, validation and contribute to documentation and testing while traveling to client sites as needed.

Manage a territory across Canberra and regional NSW to promote a cardiometabolic product. Engage GPs and specialists, build professional relationships, execute territory plans, support GP sales team obtaining key opinion leaders for educational meetings, and achieve sales targets to improve patient outcomes.

The role involves site monitoring, managing study progress, ensuring regulatory compliance, and communicating effectively with sites and project teams.

The Senior Clinical Research Associate will perform site monitoring and management tasks to ensure compliance with study protocols and regulatory guidelines, manage recruitment plans, and collaborate with study team members for project execution.

Lead and develop a monitoring/resourcing team for clinical trials, ensuring quality, targets, profitability, and compliance. Manage staffing, training, performance, client relationships, site visits, issue resolution, and continuous process improvement.