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Clinical Research Associate II - Job Opportunity at Parexel

Kowloon, Hong Kong
Full-time
Mid-level
Posted: March 18, 2025
Hybrid
HKD 420,000 - 580,000 annually based on Hong Kong CRA II market rates and multinational CRO compensation structures

Benefits

Comprehensive healthcare coverage typical of global CROs
Professional development and training programs
Global mobility opportunities
Performance-based bonus structure

Key Responsibilities

Lead site management and relationship building with clinical investigators and staff
Drive study startup activities including site qualification and regulatory documentation
Manage clinical trial documentation and regulatory compliance
Oversee site performance and ensure data quality and protocol adherence
Coordinate between sites, sponsors, and internal teams

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 Sound presentation skills Client focused approach Flexible attitude Strong computer skills including CTMS Sound interpersonal skills Time management abilities Cross-cultural work capabilities Attention to detail

Certifications

Driver's license where required
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Sauge AI Market Intelligence

Industry Trends

Increasing adoption of decentralized clinical trials requiring new technological competencies Growing emphasis on real-world evidence and adaptive trial designs Rising demand for Asia-Pacific clinical research expertise due to market expansion

Role Significance

Typically works within a study team of 5-8 members including CRAs, project managers, and data managers
Mid-level position with significant autonomy in site management and trial coordination

Key Projects

Phase II-IV clinical trials in multiple therapeutic areas Site initiation and management activities Regulatory documentation preparation and submissions Quality assurance and compliance monitoring

Success Factors

Strong interpersonal skills for site relationship management Detail-oriented approach to regulatory compliance Ability to work independently while maintaining team coordination Effective time management across multiple sites and studies

Market Demand

High demand with steady growth projected due to increasing clinical trial activity in Asia-Pacific region and ongoing pharmaceutical industry expansion

Important Skills

Critical Skills

Clinical research regulatory knowledge Site management expertise Documentation and compliance skills Stakeholder communication abilities

Beneficial Skills

Technical proficiency with clinical trial management systems Understanding of local healthcare systems Project management capabilities

Unique Aspects

Strong focus on self-driven work with limited oversight
Emphasis on cross-cultural competency for regional role
Balance of remote and on-site activities

Career Growth

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

Potential Next Roles

Senior Clinical Research Associate Clinical Trial Manager Project Manager Clinical Operations Manager

Company Overview

Parexel

Leading global Clinical Research Organization (CRO) with extensive presence in biopharmaceutical research and development

Top-tier CRO with strong market position in clinical trial management and regulatory services
Strategic APAC hub position in Hong Kong supporting regional clinical trial operations
Matrix organization emphasizing global collaboration and professional development
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