Associate Centralized Monitoring Lead

IQVIA Inc

Fully remote
Ich gcp regulatory compliance knowledge
Centralized monitoring plan development
Site visit report review and analysis
The role supports CMS leads in delivering project objectives while optimizing speed, quality, and cost of delivery

Job Summary

  • The role supports CMS leads in delivering project objectives while optimizing speed, quality, and cost of delivery.
  • Responsibilities include reviewing site visit reports, managing study metrics trending, and ensuring subject safety and data integrity.
  • The position requires acting as a technical solution specialist to gather requirements and provide inputs for continuous process improvements.

Matching Summary

The role supports CMS leads in delivering project objectives while optimizing speed, quality, and cost of delivery.

Skills & Requirements

Must-have

  • ICH GCP regulatory compliance knowledge
  • Centralized Monitoring Plan development
  • Site visit report review and analysis
  • Clinical trial data integrity assurance
  • Risk identification and mitigation strategies

Nice-to-have

  • Mentoring junior centralized monitoring staff
  • Strong cross-functional collaboration skills
  • Experience with therapeutic area specifics
  • Advanced analytical tool proficiency
  • Effective presentation and communication skills

Key Requirements

  • Bachelor's Degree in Clinical or Life Sciences
  • Minimum 4 years of relevant work experience
  • At least 2 years in centralized monitor role preferred
  • Good knowledge of ICH GCP and local regulations

Work Rights

Not specified

Tailored Resume

Cover Letter