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Clinical Research Associate (SCRA2) - Job Opportunity at IQVIA

Remote, Hong Kong
Full-time
Mid-level
Posted: May 1, 2025
Remote
HKD 420,000 - 580,000 per year based on Hong Kong market rates for experienced CRAs

Benefits

Comprehensive healthcare package typical for global CRO
Professional development and training opportunities
Global mobility opportunities
Technology allowance for remote work setup

Key Responsibilities

Lead site monitoring and quality assurance for clinical trials with direct impact on drug development timelines
Drive strategic site performance optimization and subject recruitment to meet critical study milestones
Manage regulatory compliance and documentation processes essential for trial validity
Execute comprehensive site management activities including selection, initiation, and closeout
Facilitate cross-functional collaboration to ensure trial efficiency and data integrity

Requirements

Education

High School Diploma or equivalent, Degree in scientific discipline or health care preferred

Experience

2 years of on-site monitoring experience

Required Skills

Good Clinical Practice (GCP) knowledge ICH guidelines expertise Microsoft Office proficiency Written and verbal communication skills Organizational and problem-solving skills Time and financial management skills Therapeutic and protocol knowledge

Certifications

GCP certification implied but not explicitly required
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Sauge AI Market Intelligence

Industry Trends

The clinical research industry is experiencing rapid digitalization with increased adoption of remote monitoring technologies and decentralized trials Asia-Pacific region, particularly Hong Kong, is becoming a crucial hub for clinical trials due to efficient regulatory processes and large patient populations Growing demand for experienced CRAs due to post-pandemic surge in clinical trials

Role Significance

Typically works within a team of 5-8 CRAs under a Clinical Trial Manager, supporting 4-8 active sites
Mid-level position with significant autonomy in site management and trial execution

Key Projects

Phase II-III clinical trials in major therapeutic areas Multi-center international studies Complex protocol implementation and site management initiatives

Success Factors

Strong attention to detail and quality focus in monitoring activities Excellent stakeholder management skills across sites, sponsors, and internal teams Ability to identify and escalate critical issues promptly Effective time management while handling multiple sites and studies

Market Demand

High demand with steady growth projected over next 3-5 years due to increasing clinical trial activity in APAC region

Important Skills

Critical Skills

GCP/ICH knowledge is foundational for ensuring trial compliance and quality Communication skills are essential for effective site management and stakeholder collaboration Technical proficiency with clinical trial management systems and remote monitoring tools

Beneficial Skills

Additional therapeutic area expertise Local language skills for site communication Project management capabilities Understanding of risk-based monitoring approaches

Unique Aspects

Remote work opportunity in a traditionally site-based role indicates progressive work policies
Position combines traditional monitoring with modern technology-enabled processes
Strong focus on data integrity and quality management reflects evolving regulatory environment

Career Growth

2-3 years in current role before advancement, depending on performance and business needs

Potential Next Roles

Senior Clinical Research Associate Clinical Trial Manager Clinical Operations Manager Regional Monitoring Manager

Company Overview

IQVIA

IQVIA is a global leader in clinical research and healthcare intelligence, formed from the merger of Quintiles and IMS Health

Industry leader with significant market share in clinical research services and healthcare data analytics
Strong APAC presence with Hong Kong serving as a strategic hub for regional operations
Matrix organization with emphasis on global collaboration and professional development
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