Fsp Sr Cra I

Thermo Fisher Scientific UK

United Kingdom
**
Neurology or oncology monitoring experience
Risk-based monitoring approach application
Ich-gcp guidelines and regulatory compliance
** Thermo Fisher Scientific is seeking a Senior Clinical Research Associate (Level I) for a fully remote role, focusing on clinical monitoring and site management within various therapeutic areas, particularly neurology, oncology, and rare diseases. The ideal candidate should have at least two years of relevant experience, strong problem-solving skills, and a solid understanding of ICH-GCP guidelines. **

Job Summary

  • The role involves conducting remote or on-site visits to assess protocol compliance and manage documentation for clinical trials.
  • Candidates must possess adequate neurology or oncology monitoring experience, with rare disease and pediatric experience strongly advised.
  • This position offers the opportunity to join a global team supporting top pharmaceutical companies across over 100 countries.

Matching Summary

Match Score: 75

** Thermo Fisher Scientific is seeking a Senior Clinical Research Associate (Level I) for a fully remote role, focusing on clinical monitoring and site management within various therapeutic areas, particularly neurology, oncology, and rare diseases. The ideal candidate should have at least two years of relevant experience, strong problem-solving skills, and a solid understanding of ICH-GCP guidelines. **

Skills & Requirements

Must-have

  • Neurology or oncology monitoring experience
  • Risk-based monitoring approach application
  • ICH-GCP guidelines and regulatory compliance
  • Root cause analysis and problem solving
  • On-site and remote clinical trial visits

Nice-to-have

  • Rare disease and pediatric experience advised
  • Strong collaborative relationship building skills
  • Effective communication with medical personnel
  • Experience with Clinical Trial Management Systems
  • Ability to work independently in team settings

Key Requirements

  • Bachelor's degree in life sciences or Registered Nursing certification
  • 2+ years of experience as a clinical research monitor
  • Valid driver's license where applicable

Work Rights

Not specified

Tailored Resume

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