Clinical Research Associate - Client Dedicated (fsp) Belgium

PPD (Thermo Fisher) UK

Belgium
Competitive remuneration; annual incentive plan bo...
Independent on-site clinical monitoring experience
Understanding of ich-gcp eu and fda requirements
Excellent command of english and dutch or french
The role involves performing and coordinating all aspects of the clinical monitoring process independently

Job Summary

  • The role involves performing and coordinating all aspects of the clinical monitoring process independently.
  • Candidates will benefit from award-winning training programs designed to assist with technical and professional skill development.
  • The company offers competitive remuneration, an annual incentive plan bonus, healthcare, and a range of employee benefits.

Matching Summary

The role involves performing and coordinating all aspects of the clinical monitoring process independently.

Salary

Competitive remuneration; Annual incentive plan bonus; Healthcare and employee benefits

Skills & Requirements

Must-have

  • Independent on-site clinical monitoring experience
  • Understanding of ICH-GCP EU and FDA requirements
  • Excellent command of English and Dutch or French

Nice-to-have

  • Experience in Oncology and/or Vaccines
  • Ability to thrive in multi-national project teams
  • Strong communication and interpersonal skills

Key Requirements

  • University degree in a life-sciences field
  • At least 6 months independent on-site clinical monitoring experience
  • Demonstrated understanding of medical terminology

Work Rights

Not specified

Tailored Resume

Cover Letter