Senior Clinical Research Associate - Offering Joining Bonus!

Thermo Fisher Scientific UK

Not specified; joining bonus offered; not specifie...
Fully remote
Risk-based monitoring approach
Ich-gcp guidelines knowledge
On-site and remote monitoring
The role involves performing and coordinating clinical monitoring and site management processes to ensure trial compliance with ICH-GCP guidelines

Job Summary

  • The role involves performing and coordinating clinical monitoring and site management processes to ensure trial compliance with ICH-GCP guidelines.
  • Thermo Fisher Scientific offers a global mission to make the world healthier, cleaner, and safer through life-changing therapies.
  • Candidates will play a key role in assessing investigational products, documenting observations, and resolving issues with investigative sites.

Matching Summary

The role involves performing and coordinating clinical monitoring and site management processes to ensure trial compliance with ICH-GCP guidelines.

Salary

Not specified; Joining bonus offered; Not specified

Skills & Requirements

Must-have

  • Risk-based monitoring approach
  • ICH-GCP guidelines knowledge
  • On-site and remote monitoring
  • Protocol and regulatory compliance
  • Data accuracy through SDV/SDR

Nice-to-have

  • Root cause analysis skills
  • Critical thinking and problem-solving
  • Effective written communication
  • Experience with Clinical Trial Management Systems

Key Requirements

  • Bachelor's degree in life science or Nursing certification
  • Valid driver's license
  • At least 1 year of independent CRA monitoring experience
  • Fluency in Romanian and English

Work Rights

Not specified

Tailored Resume

Cover Letter