Fsp Cra - Fully Client Dedicated Sweden

PPD (Thermo Fisher) UK

Sweden
Not specified; not specified; not specified
Fully remote
Bachelor's degree in life sciences
1 year clinical research monitor experience
Valid driver's license
You will conduct remote or on-site visits to assess protocol and regulatory compliance while managing required documentation

Job Summary

  • You will conduct remote or on-site visits to assess protocol and regulatory compliance while managing required documentation.
  • The role requires applying root cause analysis and problem-solving skills to identify site process failures and ensure corrective actions.
  • As a global team member, you will have the opportunity to perform all aspects of clinical monitoring across over 2,700 clinical trials.

Matching Summary

You will conduct remote or on-site visits to assess protocol and regulatory compliance while managing required documentation.

Salary

Not specified; Not specified; Not specified

Skills & Requirements

Must-have

  • Bachelor's degree in life sciences
  • 1 year clinical research monitor experience
  • Valid driver's license
  • ICH-GCP guidelines knowledge
  • Risk-based monitoring approach
  • Root cause analysis skills

Nice-to-have

  • Strong critical thinking abilities
  • Excellent oral and written communication
  • Ability to work independently or in teams
  • Fluency in Swedish language
  • Experience with Clinical Trial Management Systems

Key Requirements

  • Bachelor's degree in life sciences or Nursing certification
  • Minimum 1 year experience as a clinical research monitor
  • Valid driver's license where applicable

Work Rights

Not specified

Tailored Resume

Cover Letter