Jobs at IQVIA

The CRA I supports clinical research by monitoring sites, ensuring compliance with regulations, and maintaining communication with investigative sites. Responsibilities include site visits, protocol training, and documentation preparation.

Responsible for site monitoring and management in oncology clinical trials, ensuring compliance with protocols and regulations while managing site relationships and documentation.

The Associate Director will lead AI change management efforts, integrating project management and change methodologies to enhance AI adoption across the organization, train teams, and support transformation efforts through strategic partnerships.

Lead data management for complex global clinical trials, ensuring quality and compliance while mentoring staff and driving process improvements.

Lead the data management for global clinical trials, ensuring quality and compliance while overseeing teams and managing resources and timelines.

Oversee site monitoring and management, ensure compliance with protocols, and facilitate recruitment and training for clinical studies.

The role involves leading client engagements, developing business opportunities, and ensuring high client satisfaction by delivering strategic solutions in pharmaceutical market research.

The Clinical Research Associate will monitor clinical sites for adherence to protocols, ensure data integrity, manage communications, and oversee regulatory compliance throughout clinical trials.