FSP CTA (Clinical Trial Assistant) - Job Opportunity at Thermo Fisher Scientific

New Territories, Hong Kong
Full-time
Mid-level
Posted: March 23, 2025
On-site
HKD 240,000 - 320,000 per year based on Hong Kong market rates for clinical research positions

Benefits

Comprehensive healthcare coverage aligned with industry standards
Career development and training programs
Global exposure through multinational projects
Work-life balance initiatives

Key Responsibilities

Coordinate and oversee clinical trial administrative activities across multiple studies
Maintain study documentation and regulatory compliance
Support Risk-Based Monitoring (RBM) activities and quality assurance
Manage investigator site documentation and communications
Facilitate internal and external stakeholder meetings
Process and track regulatory documents and vendor relationships

Requirements

Education

Bachelor's degree preferred

Experience

2 years of relevant experience

Required Skills

Good Clinical Practice (GCP) knowledge Strong English language and grammar skills Proficiency in MS Office Clinical trial database systems expertise Project management capabilities Document management skills Multi-tasking abilities Analysis and problem-solving skills
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Sauge AI Market Intelligence

Industry Trends

Increasing adoption of decentralized clinical trials requiring enhanced administrative support and digital competencies Growing emphasis on Risk-Based Monitoring (RBM) approaches in clinical research Rising demand for data management and regulatory compliance expertise in clinical trials Expansion of Asia-Pacific clinical research market creating increased opportunities

Role Significance

Typically part of a 5-10 person clinical operations team, collaborating with global study teams
Mid-level position with significant operational responsibility in clinical trial execution

Key Projects

Multi-country clinical trial coordination Regulatory document management and compliance Site file maintenance and quality assurance Clinical trial administration process improvement

Success Factors

Strong attention to detail and organizational skills Ability to work effectively in a global matrix environment Understanding of clinical research regulations and GCP Excellent communication and stakeholder management abilities

Market Demand

High demand driven by expanding clinical research activities in Asia-Pacific region and increasing regulatory requirements

Important Skills

Critical Skills

GCP and regulatory compliance knowledge essential for maintaining trial integrity Database management skills crucial for modern clinical trial execution Communication skills vital for coordinating with global stakeholders

Beneficial Skills

Knowledge of emerging clinical trial technologies Understanding of Risk-Based Monitoring approaches Experience with electronic Trial Master File (eTMF) systems

Unique Aspects

Integration of PPD clinical research capabilities within Thermo Fisher Scientific's broader scientific ecosystem
Exposure to diverse therapeutic areas and global clinical trials
Opportunity to work with cutting-edge clinical trial technologies and processes

Career Growth

2-3 years in role before advancement opportunities

Potential Next Roles

Clinical Research Associate (CRA) Clinical Project Manager Clinical Operations 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

Fortune 500 company with strong market position in life sciences and clinical research services
Strategic location in Hong Kong serving as gateway to Asia-Pacific clinical trials
Professional, fast-paced environment with emphasis on quality and compliance
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