Clinical Research Associate

539

Not specified; market-competitive salary + benefit...
Hybrid
Ich-gcp compliance knowledge
Site monitoring and validation
Adverse event reporting
The Clinical Research Associate is accountable for ensuring study conduct at assigned sites is fully compliant with ICH/GCP, local regulations, and internal policies

Job Summary

  • The Clinical Research Associate is accountable for ensuring study conduct at assigned sites is fully compliant with ICH/GCP, local regulations, and internal policies.
  • Key responsibilities include conducting on-site and remote monitoring visits, managing study start-up and close-out activities, and maintaining accurate documentation in CTMS and eTMF systems.
  • The role offers a flexible hybrid working model, competitive compensation, and opportunities for professional growth within a supportive multicultural team environment.

Matching Summary

The Clinical Research Associate is accountable for ensuring study conduct at assigned sites is fully compliant with ICH/GCP, local regulations, and internal policies.

Salary

Not specified; Market-competitive salary and benefits package including health and wellness programs; Pension/retirement plans available

Skills & Requirements

Must-have

  • ICH-GCP compliance knowledge
  • Site monitoring and validation
  • Adverse event reporting
  • Protocol adherence expertise
  • CTMS and eTMF proficiency

Nice-to-have

  • Mentoring junior CRAs
  • Cross-functional collaboration
  • Territory development skills
  • Root cause analysis capability
  • Continuous improvement mindset

Key Requirements

  • Bachelor's degree in scientific or healthcare discipline
  • Minimum 6 months experience in monitoring activities
  • Valid driving license required
  • Fluency in local language(s) and English

Work Rights

Not specified

Tailored Resume

Cover Letter