Jobs at IQVIA

The Senior Clinical Research Associate will monitor and manage clinical trial sites to ensure compliance with protocols, regulations, and sponsor requirements, while collaborating with teams to enhance study execution.

This role involves monitoring clinical centers, ensuring compliance with study protocols, and maintaining communication with investigators. Responsibilities include site visits, participant recruitment oversight, and quality control of studies.

The Senior Clinical Research Associate will oversee clinical trial sites, ensure compliance with regulations, and manage study progress, coordinating with investigators and project teams.

The Clinical Research Associate II is responsible for monitoring oncology clinical trials, ensuring compliance, training site personnel, conducting visits, and managing documentation.

The Senior Clinical Research Associate oversees site management and monitoring activities for clinical trials, ensuring regulatory compliance and effective communication with sites to achieve project goals.

Perform monitoring and site management to ensure compliance with study protocols, regulations, and sponsor requirements, including site visits and documentation.

Home‑based CRA II responsible for monitoring Phase I–IV oncology trials (selection, initiation, monitoring, close‑out). Ensure GCP/ICH and protocol compliance, data integrity, IP and regulatory document oversight, train site staff on protocols/EDC, prepare monitoring reports, and support investigator meetings. Requires regular site communication and travel for site activities.

The Clinical Research Associate II monitors oncology clinical trials, conducts site visits, ensures compliance with regulations, and manages data integrity.

The Senior Clinical Research Associate is responsible for monitoring site activities, managing clinical trials, ensuring compliance with regulations, and mentoring clinical staff.

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.

Oversee and manage the QA program, ensuring compliance with regulations, providing support and training to development groups, and addressing audit findings while improving processes.

Support order-to-cash operations including billing, revenue recognition, AR ageing and collections, ensure GAAP compliance, assist sales handoffs, perform financial analyses, and improve processes while working with global stakeholders using SAP and Excel.

Provide FP&A support including monthly forecasts, budgeting, variance analysis and management reporting. Reconcile data across ERP/CRM systems, prepare presentations for senior management, recommend system improvements, support M&A integrations, and perform ad-hoc financial analyses.

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.

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.