Jobs at IQVIA

Provide advanced technical support for Veeva applications, resolving issues, managing environments, and ensuring optimal performance for Life Sciences clients. Collaborate with teams and document processes while staying updated on Veeva products.

Lead execution of global oncology clinical trials ensuring ICH/GCP compliance, meeting recruitment targets, managing clinical risk and EAC budgets, assuring quality, coordinating stakeholders, coaching clinical teams, supporting proposals, and mentoring staff as needed.

Manage end-to-end client-specific patient support programs: set up, launch, monitor performance, escalate risks, produce client reports, and lead a team of caseworkers ensuring QA, KPIs, SOP compliance, and continuous improvement.

The Clinical Scientist will oversee and ensure data quality in clinical trials, conduct protocol reviews, develop training materials, and communicate with stakeholders.

Client-focused Technology Analyst responsible for designing, developing and delivering data and technology solutions for life sciences clients. Reviews requirements, performs qualitative/quantitative analyses, crafts documentation and client presentations, supports solution implementation, and follows up to ensure client satisfaction. Develops consulting skills, market knowledge, and begins to build practice-specific subject matter expertise while identifying business opportunities.

Serve as a client-focused technology analyst for life sciences customers: gather and analyze requirements, design and deliver data-driven solutions, create documentation and client reports, recommend improvements, support client satisfaction and identify business opportunities while developing consulting and market expertise.

The Product Strategist will lead digital engagement solutions, develop new capabilities, manage client relationships, and ensure high satisfaction while leveraging data and analytics for marketing strategies.

The Senior Clinical Research Associate is responsible for site management, monitoring visits, training staff, and ensuring compliance with regulatory requirements in clinical research.