This role offers opportunities to plan and progress your career in the direction you choose, with exposure to wider opportunities like operations management and project management
Job Summary
This role offers opportunities to plan and progress your career in the direction you choose, with exposure to wider opportunities like operations management and project management.
Your responsibilities will include performing site selection, initiation, monitoring, and close-out visits, as well as managing progress by tracking regulatory submissions and data query resolution.
Joining IQVIA will give you access to cutting-edge in-house technology and provide opportunities to work on global projects/trials, building a flexible, meaningful, and fulfilling career.
Matching Summary
This role offers opportunities to plan and progress your career in the direction you choose, with exposure to wider opportunities like operations management and project management.
Skills & Requirements
Must-have
Site selection and monitoring
Regulatory submission tracking
GCP knowledge
English language proficiency
Collaboration and communication
Nice-to-have
Career development opportunities
Flexible work schedules
Cutting-edge in-house technology
Global project experience
Key Requirements
University degree in scientific discipline or healthcare
At least 1 year of on-site monitoring experience
Good knowledge of GCP and clinical research regulatory requirements