Experienced Cra

PPD (Thermo Fisher) UK

Sweden
Fully remote
Risk-based monitoring approach
Ich-gcp guidelines
Protocol and regulatory compliance
As part of our global team, you’ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process

Job Summary

  • As part of our global team, you’ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process.
  • As a Senior Clinical Research Associate, you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation.
  • We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.

Matching Summary

As part of our global team, you’ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process.

Skills & Requirements

Must-have

  • Risk-based monitoring approach
  • ICH-GCP guidelines
  • Protocol and regulatory compliance
  • Investigational product assessment
  • Site processes specialist

Nice-to-have

  • Collaborative environment
  • Work-life balance
  • Accelerate delivery of therapeutics

Key Requirements

  • 3+ years as a clinical research monitor
  • Bachelor's degree in life sciences or equivalent
  • Valid driver's license
  • Experience in all study phases
  • Strong Neuroscience experience

Work Rights

Not specified

Tailored Resume

Cover Letter