Central Monitor - Fsp

Parexel

Remote
Fully remote
Data surveillance
Risk-based quality management
Clinical trial oversight
The Central Monitor plays a key role in overseeing clinical trials through centralized monitoring activities

Job Summary

  • The Central Monitor plays a key role in overseeing clinical trials through centralized monitoring activities.
  • This role ensures data quality, identifies potential risks, and enhances trial oversight.
  • The CM collaborates with cross-functional teams to ensure compliance with study protocols and regulatory requirements.

Matching Summary

The Central Monitor plays a key role in overseeing clinical trials through centralized monitoring activities.

Skills & Requirements

Must-have

  • Data Surveillance
  • Risk-Based Quality Management
  • Clinical trial oversight

Nice-to-have

  • Strong communication skills
  • Proactive problem-solving
  • Collaboration with cross-functional teams

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