Fsp Cra (sponsor: Gsk) ─ With Sign-on Bonus

Thermo Fisher Scientific UK

Sign-on bonus: available; base: not specified; ben...
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Risk-based monitoring approach
Ich-gcp and kgcp requirements understanding
1-2 years independent monitoring experience
** Thermo Fisher Scientific is seeking a Clinical Research Associate (Level II) to join their team in a fully remote role, focusing on clinical monitoring and site management for various pharmaceutical sponsors, including GSK. The position offers a sign-on bonus and involves ensuring compliance with protocols and regulations while maintaining strong relationships with investigational sites. **

Job Summary

  • This role offers the opportunity to perform and coordinate all aspects of clinical monitoring and site management for a global team supporting top pharmaceutical companies.
  • The Clinical Research Associate will conduct remote or on-site visits to assess protocol compliance, manage documentation, and ensure data reliability through rigorous review processes.
  • Candidates must possess at least 1-2 years of independent monitoring experience in clinical development phases I-III and demonstrate a strong understanding of ICH-GCP guidelines.

Matching Summary

Match Score: 75

** Thermo Fisher Scientific is seeking a Clinical Research Associate (Level II) to join their team in a fully remote role, focusing on clinical monitoring and site management for various pharmaceutical sponsors, including GSK. The position offers a sign-on bonus and involves ensuring compliance with protocols and regulations while maintaining strong relationships with investigational sites. **

Salary

Sign-on Bonus: Available; Base: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Risk-based monitoring approach
  • ICH-GCP and KGCP requirements understanding
  • 1-2 years independent monitoring experience
  • Protocol and regulatory compliance assessment
  • Root cause analysis and problem solving

Nice-to-have

  • Critical thinking and investigative mindset
  • Effective communication with medical personnel
  • Collaborative relationship building skills
  • Adaptability in diverse scenarios
  • Process improvement contributions

Key Requirements

  • Bachelor's degree in life sciences or Registered Nursing certification
  • 1-2 years of independent clinical monitoring experience
  • Fluency in English language
  • Knowledge of ICH-GCP and KGCP requirements

Work Rights

Not specified

Tailored Resume

Cover Letter