Jobs at IQVIA

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

Lead and manage clinical project teams delivering complex, global multi-regional studies and programs. Develop and operationalize project delivery strategy, oversee study execution, manage risk, finances, scope changes and customer relationships, and drive cross-functional collaboration, quality, and continuous improvement. Mentor project staff and support business development activities including RFPs and bid defenses.

The Clinical Research Coordinator performs complex clinical procedures, coordinates studies, ensures participant safety, updates knowledge on practices, and supports study logistics.

The role involves providing systems expertise, defining system requirements, solving complex problems, and guiding less-experienced analysts, focusing on enhancing business systems to better serve clients and internal needs.

The Associate Consultant will provide high-quality analytical input for client projects in life sciences, assisting with problem analysis, developing solutions, and managing data. Responsibilities include analysis, presentation preparation, and managing multiple priorities in a collaborative environment.

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.

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.

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.

Manage site activation and regulatory activities for clinical trials, ensuring compliance and timely project delivery, while overseeing budgets and resource allocation.

The Associate Consultant will provide analytical support for client projects in life sciences, assist in developing proposals, conduct quantitative analyses, and communicate findings to stakeholders, while working collaboratively in a team environment.