Centralized Monitoring Asst

IQVIA

Onsite
Clinical research experience
Good clinical practice knowledge
Microsoft excel proficiency
The role involves providing administrative support to the clinical study management team under supervision

Job Summary

  • The role involves providing administrative support to the clinical study management team under supervision.
  • Candidates are responsible for monitoring site performance and identifying risks to ensure study compliance.
  • The position requires adherence to Good Clinical Practice guidelines and effective communication with clients.

Matching Summary

The role involves providing administrative support to the clinical study management team under supervision.

Skills & Requirements

Must-have

  • Clinical research experience
  • Good Clinical Practice knowledge
  • Microsoft Excel proficiency
  • Data entry skills
  • Risk identification capabilities

Nice-to-have

  • Strong communication skills
  • Time management abilities
  • Detail-oriented approach
  • Client relationship building
  • Team collaboration skills

Key Requirements

  • Minimum 2 years work experience
  • 6 months relevant clinical experience
  • Graduate or Post Graduate in Life Sciences
  • Knowledge of ICH-GCP regulations

Work Rights

Not specified

Tailored Resume

Cover Letter