Global Program Analyst at IQVIA

Beijing, Beijing, China

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical Research, Life Sciences, HealthcareIndustries

Requirements

Bachelor’s degree
Minimum 2 years of PMA experience in clinical research industry
Knowledgeable in clinical development processes
Able to communicate effectively in English

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

Skills

Key technologies and capabilities for this role

clinical trial operationsvendor managementPMAclinical researchclinical developmentSOPsdatabase managementfinancial reportingprocurementcompliance reviews

Questions & Answers

Common questions about this position

What qualifications are required for the Global Program Analyst role?

Candidates need a Bachelor’s degree, minimum 2 years of PMA experience in the clinical research industry, knowledge of clinical development processes, and effective English communication skills.

Is the salary specified for this position?

This information is not specified in the job description.

What is the employment type for this role?

The position is full time.

What does IQVIA do as a company?

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries, creating intelligent connections to accelerate medical treatments and improve patient outcomes.

What experience makes a strong candidate for this role?

A strong candidate will have at least 2 years of PMA experience in the clinical research industry, along with knowledge of clinical development processes; for advanced roles, experience mentoring juniors and handling complex issues is beneficial.

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters

1998Year Founded

$3,526MTotal Funding

POST_IPO_EQUITYCompany Stage

Cybersecurity, Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.

Proliferation of disparate technological solutions causes technology overload in clinical trials.

Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.

The company offers privacy-enhancing technologies to protect individual patient data.

IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.

AI-driven drug discovery accelerates identification of potential drug candidates.

Expansion of telemedicine facilitates remote patient monitoring and data collection.

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