Hong Kong Fsp Cra

Thermo Fisher Scientific UK

Competitive remuneration; annual incentive plan bo...
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Risk-based monitoring approach
Ich-gcp guidelines compliance
Root cause analysis skills
** Thermo Fisher Scientific is seeking a Clinical Research Associate (CRA) based in Hong Kong to coordinate clinical monitoring and site management processes in clinical trials. The position emphasizes ensuring compliance with protocols and regulations while fostering relationships with investigational sites, all within a fully remote work structure. **

Job Summary

  • The role involves performing and coordinating all aspects of clinical monitoring and site management to ensure protocol compliance.
  • Thermo Fisher Scientific offers competitive remuneration, an annual incentive plan bonus, healthcare, and outstanding career development prospects.
  • Employees are expected to maintain audit readiness and facilitate effective communication between investigative sites, the client company, and the project team.

Matching Summary

Match Score: 75

** Thermo Fisher Scientific is seeking a Clinical Research Associate (CRA) based in Hong Kong to coordinate clinical monitoring and site management processes in clinical trials. The position emphasizes ensuring compliance with protocols and regulations while fostering relationships with investigational sites, all within a fully remote work structure. **

Salary

Competitive remuneration; Annual incentive plan bonus; Healthcare and employee benefits

Skills & Requirements

Must-have

  • Risk-based monitoring approach
  • ICH-GCP guidelines compliance
  • Root cause analysis skills
  • On-site and remote monitoring
  • Investigational product inventory review

Nice-to-have

  • Critical thinking and problem solving
  • Effective oral and written communication
  • Collaborative relationship building
  • Process improvement initiatives
  • Flexible and adaptable work style

Key Requirements

  • Bachelor's degree in life sciences or Registered Nursing certification
  • 2+ years experience as a clinical research monitor
  • Proficiency with Microsoft Office and Clinical Trial Management Systems

Work Rights

Not specified

Tailored Resume

Cover Letter