Fsp Sr Cra I

PPD (Thermo Fisher)

Remote, United Kingdom
**
Risk-based monitoring approach
Ich-gcp guidelines
Protocol and regulatory compliance
** The job posting is for a Senior Clinical Research Associate (Level I) at PPD (Thermo Fisher), emphasizing remote work flexibility and a focus on monitoring clinical trials in neurology, oncology, and rare diseases. The ideal candidate should have at least two years of relevant experience and strong knowledge of clinical monitoring practices and ICH GCP guidelines. **

Job Summary

  • Perform and coordinate all aspects of the clinical monitoring and site management process.
  • Conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation.
  • Ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability.

Matching Summary

Match Score: 75

** The job posting is for a Senior Clinical Research Associate (Level I) at PPD (Thermo Fisher), emphasizing remote work flexibility and a focus on monitoring clinical trials in neurology, oncology, and rare diseases. The ideal candidate should have at least two years of relevant experience and strong knowledge of clinical monitoring practices and ICH GCP guidelines. **

Skills & Requirements

Must-have

  • Risk-based monitoring approach
  • ICH-GCP guidelines
  • Protocol and regulatory compliance
  • Site processes specialist
  • Neurology monitoring experience
  • Oncology monitoring experience

Nice-to-have

  • Rare disease experience
  • Pediatric experience
  • Root-cause analysis skills
  • Critical thinking and problem-solving

Key Requirements

  • 2+ years as a clinical research monitor
  • Bachelor's degree in life sciences or equivalent
  • Valid driver's license where applicable

Work Rights

Not specified

Tailored Resume

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