Associate Clinical Project Manager, Sponsor Dedicated

IQVIA UK

Base: $68,400.00 - $232,800.00 annualized; bonus/e...
2 years clinical trial management experience
Drafting and managing informed consent process
Managing site selection and patient recruitment strategies
This sponsor-dedicated role provides country-level oversight of clinical trials from study start-up through database lock and closeout

Job Summary

  • This sponsor-dedicated role provides country-level oversight of clinical trials from study start-up through database lock and closeout.
  • Candidates must have expertise in drafting informed consent processes, managing site selection, and driving risk-based mitigation plans.
  • The position requires two years of clinical trial management experience within a role accountable for driving local trial activities at the regional level.

Matching Summary

This sponsor-dedicated role provides country-level oversight of clinical trials from study start-up through database lock and closeout.

Salary

Base: $68,400.00 - $232,800.00 annualized; Bonus/Equity: Dependent on position offered; Benefits: Health, welfare, and other benefits included

Skills & Requirements

Must-have

  • 2 years clinical trial management experience
  • drafting and managing informed consent process
  • managing site selection and patient recruitment strategies
  • monitoring visit reports and risk-based mitigation plans
  • knowledge of ICH GCP and local regulatory standards

Nice-to-have

  • strong written and verbal communication skills
  • ability to handle conflicting priorities effectively
  • experience with vendor management activities
  • broad protocol and therapeutic knowledge
  • cross-cultural awareness for global collaboration

Key Requirements

  • Bachelor's Degree in life sciences or related field
  • 2 years clinical trial management experience
  • Intermediate level knowledge of clinical trial conduct principles

Work Rights

Must reside in the same country where the job is located

Tailored Resume

Cover Letter