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The Senior Clinical Programmer will develop, test, and validate clinical data applications, ensuring compliance with CDISC SDTM standards, and mentor junior programmers.

Oversee data management for global clinical trials, ensuring quality and compliance, managing resources, budgets, and mentoring staff.

Manage compliance audits for clinical trial laboratory systems, oversee quality assurance processes, and ensure regulatory compliance within IQVIA divisions. Lead teams, evaluate audit findings, and maintain quality management systems while collaborating with IT and QA functions.

The role involves managing national accounts, developing business strategies, ensuring promotional activities, achieving profitability targets, and maintaining relationships with clients and stakeholders.

The Site Research Assistant supports clinical research studies, manages documentation, data entry, patient enrollment, and coordinates logistics for trials.

Responsible for financial oversight of clinical trials, managing country budgets, ensuring compliance with regulations, and supporting submissions and approvals.

The Key Account Manager will build targeted account plans, secure access with hospital pharmacies, and deliver strategic events for effective prescribing action.

Oversee end-to-end data management for global clinical trials, ensuring quality and compliance while leading cross-functional teams and managing timelines and budgets.

The Clinical Research Associate will monitor sites for Oncology studies, ensuring compliance with protocols and managing communications and documentation.

Manage site activation and regulatory activities for clinical trials, ensuring compliance with regulations and project timelines, while providing support and guidance across programs.