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FSP CTA - Job Opportunity at Thermo Fisher Scientific

New Territories, Hong Kong
Full-time
Mid-level
Posted: March 14, 2025
On-site
HKD 280,000 - 350,000 per year based on Hong Kong market rates for clinical research positions

Benefits

Comprehensive clinical research training program
Professional development opportunities
Global exposure working on international clinical trials
Career advancement pathways in clinical research
Access to cutting-edge clinical trial technologies

Key Responsibilities

Coordinate and execute clinical trial administrative activities across 100+ countries
Manage regulatory documentation and compliance processes for clinical studies
Support quality assurance through systematic file reviews and audit preparation
Facilitate cross-functional communication and documentation management
Maintain critical study metrics and vendor relationships
Execute site documentation and supply coordination

Requirements

Education

Bachelor's degree preferred

Experience

2 years of relevant experience

Required Skills

Good Clinical Practices knowledge Strong English language and grammar skills Proficient MS Office skills Clinical trial database systems expertise Project management capabilities Attention to detail Multi-tasking ability Analytical skills Communication skills
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Sauge AI Market Intelligence

Industry Trends

The clinical trial industry is experiencing rapid digitalization with increased adoption of decentralized trial methodologies and eClinical solutions. Growing emphasis on Risk-Based Monitoring (RBM) approaches is creating new specialized roles in clinical trial administration. Asia-Pacific region is seeing significant growth in clinical trial activities, particularly in specialized therapeutic areas.

Role Significance

Typically part of a 5-10 person clinical operations team, collaborating with larger cross-functional groups of 20-30 members
Mid-level position with significant operational responsibility in clinical trial execution and quality assurance

Key Projects

Multi-country clinical trial coordination Regulatory documentation management Site initiation and maintenance support Quality assurance and audit preparation Clinical trial metrics analysis and reporting

Success Factors

Strong attention to detail and organizational skills for managing complex documentation requirements Ability to work effectively in a global matrix organization Understanding of clinical research regulations and GCP guidelines Excellent communication skills for coordinating with multiple stakeholders Adaptability to evolving clinical trial technologies and processes

Market Demand

High demand with steady growth projected due to increasing clinical trial activities in Asia-Pacific region and expansion of decentralized trial methodologies

Important Skills

Critical Skills

GCP and regulatory knowledge essential for ensuring compliance and quality in clinical trials Database management skills crucial for handling complex clinical trial data Project coordination capabilities vital for managing multiple stakeholder relationships

Beneficial Skills

Knowledge of emerging clinical trial technologies Understanding of Risk-Based Monitoring approaches Experience with eTMF systems Local language skills for regional coordination

Unique Aspects

Integration of PPD clinical research portfolio provides unique career development opportunities
Exposure to diverse therapeutic areas and global clinical trials
Focus on innovative clinical trial methodologies including decentralized trials
Strong emphasis on professional development and internal advancement

Career Growth

2-3 years in current role before advancement opportunities, with potential fast-track progression based on performance

Potential Next Roles

Clinical Trial Manager Clinical Research Associate Clinical Operations Manager Project Manager Quality Assurance Specialist

Company Overview

Thermo Fisher Scientific

Thermo Fisher Scientific is a global leader in serving science, with significant presence in clinical research through its PPD clinical research portfolio

Industry leader with over 100,000 employees and extensive global presence in life sciences and clinical research
Strong Asia-Pacific presence with significant investment in clinical research capabilities
Professional environment focused on scientific advancement with emphasis on quality and compliance
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