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IQVIA is seeking an Associate Site Contract Specialist to support regulatory submissions and contract activities for clinical trials. You will interact with internal teams and external sites to ensure timely and compliant contracts, budgets, and amendments.
This role emphasizes strong communication, organization, and attention to regulatory details. Join IQVIA’s global team, supporting multiple projects, with standard Monday–Friday schedules and office environments.
IQVIA is seeking an Associate Site Contract Specialist to support regulatory submissions and contract activities for clinical trials. You will interact with internal teams and external sites to ensure timely and compliant contracts, budgets, and amendments.
This role emphasizes strong communication, organization, and attention to regulatory details. Join IQVIA’s global team, supporting multiple projects, with standard Monday–Friday schedules and office environments.