Clinical Trial Manager - Sponsor Dedicated

IQVIA UK

Not specified; not specified; not specified
2 years local trial management experience
Strong knowledge of ich-gcp regulations
Experience as clinical research associate
The role involves providing end-to-end project management for clinical trials from start-up through closeout activities at the local level

Job Summary

  • The role involves providing end-to-end project management for clinical trials from start-up through closeout activities at the local level.
  • Candidates must ensure study compliance by maintaining trial management systems and participating in Health Authority inspections and internal audits.
  • The position requires acting as the primary company contact to monitor patient recruitment rates and manage local team progress against timelines.

Matching Summary

The role involves providing end-to-end project management for clinical trials from start-up through closeout activities at the local level.

Salary

Not specified; Not specified; Not specified

Skills & Requirements

Must-have

  • 2 years local trial management experience
  • Strong knowledge of ICH-GCP regulations
  • Experience as Clinical Research Associate
  • Budget forecasting and financial management skills
  • Proficiency in English and country language

Nice-to-have

  • Specific therapeutic area experience
  • Willingness to travel for business needs
  • Strong decision-making capabilities
  • Experience with Health Authority inspections

Key Requirements

  • BA/BS degree in health or science field
  • Minimum 2 years pharmaceutical or CRO experience
  • Previous experience as Clinical Research Associate

Work Rights

Not specified

Tailored Resume

Cover Letter