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Clinical Research Associate I - Job Opportunity at Parexel

Kowloon, Hong Kong
Full-time
Entry-level
Posted: March 4, 2025
Hybrid
HKD 300,000 - 450,000 per year based on Hong Kong market rates for entry-level CRA positions

Benefits

Pharmaceutical industry competitive benefits package
Professional development opportunities
Global exposure in clinical research
Career advancement pathways

Key Responsibilities

Lead site identification and qualification processes for clinical trials
Manage regulatory documentation and submissions
Oversee site performance and compliance monitoring
Coordinate between research sites and stakeholders
Ensure data quality and integrity throughout trial lifecycle

Requirements

Education

Degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification or other equivalent experience

Experience

Previous relevant work experience preferred

Required Skills

Problem solving skills Independent work capability Presentation skills Client focused approach Professional interaction abilities Flexible attitude Task management capabilities Matrix environment adaptability Strong computer skills Communication skills Time management abilities Cross-cultural work capabilities Virtual team collaboration Detail orientation Valid driver's license where required
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Sauge AI Market Intelligence

Industry Trends

Increasing adoption of decentralized clinical trials driving demand for tech-savvy CRAs Growing focus on Asia-Pacific region as a key clinical research market Rising complexity in regulatory compliance requirements across multiple jurisdictions Shift towards risk-based monitoring approaches in clinical trials

Role Significance

Typically works within a matrix team of 5-10 professionals including senior CRAs, project managers, and data managers
Entry-level position with significant responsibility for trial execution and site management

Key Projects

Phase I-IV clinical trials Site initiation and monitoring activities Regulatory documentation management Site staff training and support

Success Factors

Strong attention to detail and protocol adherence Excellent communication skills across cultural contexts Ability to build and maintain site relationships Technical proficiency with clinical trial management systems Adaptability to changing regulatory requirements

Market Demand

High demand with strong growth trajectory due to expanding clinical trial activities in Asia-Pacific region and increasing regulatory requirements

Important Skills

Critical Skills

Clinical trial documentation expertise Regulatory compliance knowledge Site relationship management Data quality assessment capabilities Problem-solving abilities

Beneficial Skills

Technical proficiency with EDC systems Understanding of ICH-GCP guidelines Project management skills Language skills relevant to Asia-Pacific region

Unique Aspects

Strong focus on technology integration in clinical trial management
Extensive global network providing broad exposure
Structured career development pathway
Access to diverse therapeutic areas and trial types

Career Growth

Typical progression to CRA II within 2-3 years with demonstrated performance

Potential Next Roles

Clinical Research Associate II Senior Clinical Research Associate Clinical Trial Manager Clinical Operations Manager

Company Overview

Parexel

Parexel is a leading global Contract Research Organization (CRO) with extensive presence in clinical research services

Top-tier CRO with strong market position in Asia-Pacific region
Strategic Hong Kong location serving as hub for Asian clinical trial operations
Matrix organization emphasizing global collaboration and professional development
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