Centralized Monitoring Asst

IQVIA UK

Onsite
Clinical research experience
Microsoft excel proficiency
Good clinical practice knowledge
IQVIA UK is seeking a Centralized Monitoring Assistant to provide administrative support to clinical study management teams. The role involves tasks such as report preparation, system maintenance, and monitoring site performance, requiring a background in life sciences and strong communication skills

Job Summary

  • The role involves providing study-level administrative support to the clinical study management team under supervision.
  • Responsibilities include periodic review of site-level Key Risk Indicators and facilitating early identification of risks during study conduct.
  • Candidates must adhere to International Conference on Harmonisation Good Clinical Practice guidelines and relevant local laws.

Matching Summary

Match Score: 75

IQVIA UK is seeking a Centralized Monitoring Assistant to provide administrative support to clinical study management teams. The role involves tasks such as report preparation, system maintenance, and monitoring site performance, requiring a background in life sciences and strong communication skills.

Skills & Requirements

Must-have

  • Clinical research experience
  • Microsoft Excel proficiency
  • Good Clinical Practice knowledge
  • Data entry skills
  • Site performance monitoring

Nice-to-have

  • Strong communication skills
  • Detail-oriented approach
  • Time management abilities
  • Effective listening skills
  • Client relationship building

Key Requirements

  • Minimum 2 years work experience
  • Minimum 6 months relevant experience
  • Graduate or Post Graduate in Life Sciences
  • Basic knowledge of GCP regulations
  • English language proficiency

Work Rights

Not specified

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