Associate Clinical Project Manager, Sponsor Dedicated

IQVIA UK

United Kingdom
Base: $68,400.00 - $232,800.00; bonus/equity: ince...
Country-level oversight of clinical trials
High-quality data delivery
Regulatory compliance
This sponsor-dedicated role provides country-level oversight of clinical trials from study start-up through database lock and closeout, ensuring high-quality data delivery and regulatory compliance

Job Summary

  • This sponsor-dedicated role provides country-level oversight of clinical trials from study start-up through database lock and closeout, ensuring high-quality data delivery and regulatory compliance.
  • The position collaborates closely with cross-functional teams to support trial execution, maintain inspection readiness, and uphold GCP, SOP, and local regulatory standards.
  • Associate Clinical Project Managers are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster.

Matching Summary

This sponsor-dedicated role provides country-level oversight of clinical trials from study start-up through database lock and closeout, ensuring high-quality data delivery and regulatory compliance.

Salary

Base: $68,400.00 - $232,800.00; Bonus/Equity: Incentive plans, bonuses may be offered; Benefits: Range of health and welfare and/or other benefits

Skills & Requirements

Must-have

  • country-level oversight of clinical trials
  • high-quality data delivery
  • regulatory compliance
  • informed consent process management
  • site selection
  • patient recruitment strategies
  • monitoring visit reports
  • risk-based mitigation plans
  • GCP, SOP, and local regulatory standards
  • cross-functional team collaboration

Nice-to-have

  • fast-paced environment
  • evolving priorities
  • therapeutic knowledge desired
  • high awareness of cultural differences
  • customer service skills

Key Requirements

  • 2 years clinical trial management experience
  • Bachelor's Degree in life sciences or related field
  • Knowledge of clinical trial conduct
  • ICH GCP and relevant local laws knowledge
  • Intermediate level knowledge of job area principles

Work Rights

Must reside in the same country where the job is located

Tailored Resume

Cover Letter