Clinical Research Associate - Fsp

PPD (Thermo Fisher)

UK
Fully remote
Bachelor's degree in life sciences
2 years clinical monitoring experience
Valid driver's license
You will conduct remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for top pharmaceutical companies

Job Summary

  • You will conduct remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for top pharmaceutical companies.
  • The role requires applying root cause analysis and critical thinking to identify site process failures and implement corrective actions to ensure data accuracy.
  • As part of a global team, you will facilitate effective communication between investigative sites, the client company, and internal project teams.

Matching Summary

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

Skills & Requirements

Must-have

  • Bachelor's degree in life sciences
  • 2 years clinical monitoring experience
  • Valid driver's license
  • ICH-GCP guidelines knowledge
  • Risk-based monitoring approach

Nice-to-have

  • Critical thinking and problem-solving skills
  • Collaborative relationship building
  • Process improvement initiatives
  • Flexible and adaptable mindset
  • Strong written communication standards

Key Requirements

  • Bachelor's degree in life sciences
  • Registered Nursing certification or equivalent
  • Minimum 2 years clinical monitoring experience
  • Valid driver's license where applicable

Work Rights

Not specified

Tailored Resume

Cover Letter