Job Description

Global Program Analyst

Pekín, China R1515170 Híbrido

Pekín, China| Dalian, China

Descripción del puesto

Responsibilities

•Support global clinical trial operations and manage vendor-supported services to ensure compliance, timelines, and budget adherence.

•Act as the primary point of contact for study teams and external vendors, driving smooth execution of programs.

•Oversee participant reimbursement and travel assistance plans; review and process medical expense reimbursement requests in line with SOPs and regulations.

•Maintain and update databases for tracking requests and payments; provide data for financial and operational reporting.

•Collaborate with procurement on work orders and vendor management; facilitate compliance reviews and approvals.

•For advanced roles: mentor junior team members, deliver reports to leadership, and resolve complex issues proactively.

Qualifications

•Bachelor’s degree

•Minimum 2 years of PMA experience in clinical research industry

•Knowledgeable in clinical development processes.

•Able to communicate effectively in English

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

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