Central Monitor - Fsp

Parexel

Remote
Fully remote
Data surveillance
Risk-based monitoring
Clinical trial oversight
At Parexel, we are committed to improving the world's health through clinical trials and regulatory consulting

Job Summary

  • At Parexel, we are committed to improving the world's health through clinical trials and regulatory consulting.
  • The Central Monitor plays a key role in ensuring data quality and identifying potential risks in clinical trials.
  • This position involves collaboration with various teams to enhance trial oversight and compliance with regulatory requirements.

Matching Summary

At Parexel, we are committed to improving the world's health through clinical trials and regulatory consulting.

Skills & Requirements

Must-have

  • Data Surveillance
  • Risk-Based Monitoring
  • Clinical Trial Oversight

Nice-to-have

  • Strong analytical skills
  • Collaboration with cross-functional teams
  • Experience in transformation

Key Requirements

  • University degree in life science
  • ≥ 5 years of pharmaceutical industry experience
  • Strong clinical experience in clinical trial development

Work Rights

Not specified

Tailored Resume

Cover Letter